Abstract
The human T-cell lymphotropic virus type 1 (HTLV-1) is part of the family of retroviruses. Its prevalence is higher in Japan, the Caribbean basin, and some parts of Africa, South America, and the Middle East. The transmission is dependent on the transfusion of non-leukocyte depleted contaminated blood products, vertical transmission (especially by breastfeeding), and sexual intercourse mainly from male to female. The majority of patients are asymptomatic carriers, but 4–9% of patients can be complicated by the appearance of HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP) or adult T-cell leukemia/lymphoma (ATLL). Also, there is an increasing amount of literature that relates HTLV-1 infection with other inflammatory disorders such as uveitis, arthritis, Sjögren’s syndrome, dermatitis, thyroiditis, bronchiolitis-alveolitis-pneumonitis, myositis, nephritis, and hepatitis – cholangitis. However, there is no exact data regarding the prevalence or incidence of these manifestations or specific treatment for them.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Similar content being viewed by others
References
Hlela C, Shepperd S, Khumalo NP, Taylor GP. The prevalence of human T-cell lymphotropic virus type 1 in the general population is unknown. AIDS Rev [Internet]. 2009;11(4):205–14.. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19940947.
Francki RIB, Fauquet CM, Knudson DL, Brown F. Classification and Nomenclature of viruses: fifth report of the international committee on taxonomy of viruses. Virology division of the international union of microbiological societies [Internet]. Vienna: Springer; 2012. (Archives of Virology. Supplementa).
Gallo RC. History of the discoveries of the first human retroviruses: HTLV-1 and HTLV-2. Oncogene. 2005;24(39):5926–30.
Gessain A, Cassar O. Epidemiological aspects and world distribution of HTLV-1 infection. Front Microbiol. 2012;3:388.
Gonçalves DU, Proietti FA, Ribas JGR, Araújo MG, Pinheiro SR, Guedes AC, et al. Epidemiology, treatment, and prevention of human T-cell leukemia virus type 1-associated diseases. Clin Microbiol Rev. 2010;23(3):577–89.
Martin F, Taylor GP, Jacobson S. Inflammatory manifestations of HTLV-1 and their therapeutic options. Expert Rev Clin Immunol. 2014;10(11):1531–46.
Bangham CRM, Araujo A, Yamano Y, Taylor GP. HTLV-1-associated myelopathy/tropical spastic paraparesis. Nat Rev Dis Prim. 2015;1:15012.
Hewitt PE, Davison K, Howell DR, Taylor GP. Human T-lymphotropic virus lookback in NHS Blood and Transplant (England) reveals the efficacy of leukoreduction. Transfusion. 2013;53(10):2168–75.
Chen YC, Wang CH, Su IJ, Hu CY, Chou MJ, Lee TH, et al. Infection of human T-cell leukemia virus type I and development of human T-cell leukemia lymphoma in patients with hematologic neoplasms: a possible linkage to blood transfusion. Blood. 1989;74(1):388–94.
Armstrong MJ, Corbett C, Rowe IA, Taylor GP, Neuberger JM. HTLV-1 in solid-organ transplantation: current challenges and future management strategies. Transplantation. 2012;94(11):1075–84.
Glowacka I, Korn K, Potthoff SA, Lehmann U, Kreipe HH, Ivens K, et al. Delayed seroconversion and rapid onset of lymphoproliferative disease after transmission of human t-cell lymphotropic virus type 1 from a multiorgan donor. Clin Infect Dis. 2013;57(10):1417–24.
Dourado I, Andrade T, Carpenter CL, Galvão-Castro B. Risk factors for human T-cell lymphotropic virus type I among injecting drug users in Northeast Brazil: possibly greater efficiency of male to female transmission. Mem Inst Oswaldo Cruz. 1999;94(1):13–8.
Poljak M, Bednarik J, Rednak K, Seme K, Kristancic L, Celan-Lucu B. Seroprevalence of human T-cell leukaemia/lymphoma virus type I (HTLV-I) in pregnant women, patients attending venereological outpatient services and intravenous drug users from Slovenia. Folia Biol (Praha) [Internet]. 1998;44(1):23–5.. Available from: http://www.ncbi.nlm.nih.gov/pubmed/10730871.
de Thé G, Bomford R. An HTLV-I vaccine: why, how, for whom? AIDS Res Hum Retroviruses [Internet]. 1993;9(5):381–6.. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8318266.
Ando Y, Matsumoto Y, Nakano S, Saito K, Kakimoto K, Tanigawa T, et al. Long-term follow-up study of vertical HTLV-I infection in children breastfed by seropositive mothers. J Infect [Internet]. 2003;46(3):177–9.. Available from: http://www.ncbi.nlm.nih.gov/pubmed/12643867.
Murphy EL, Figueroa JP, Gibbs WN, Holding-Cobham M, Cranston B, Malley K, et al. Human T-lymphotropic virus type I (HTLV-I) seroprevalence in Jamaica. I. Demographic determinants. Am J Epidemiol [Internet]. 1991;133(11):1114–24.. Available from: http://www.ncbi.nlm.nih.gov/pubmed/2035515.
Dumas M, Houinato D, Verdier M, Zohoun T, Josse R, Bonis J, et al. Seroepidemiology of human T-cell lymphotropic virus type I/II in Benin (West Africa). AIDS Res Hum Retroviruses [Internet]. 1991;7(5):447–51.. Available from: http://www.ncbi.nlm.nih.gov/pubmed/1873079
Maloney EM, Ramirez H, Levin A, Blattner WA. A survey of the human T-cell lymphotropic virus type I (HTLV-I) in south-western Colombia. Int J Cancer [Internet]. 1989;44(3):419–23.. Available from: http://www.ncbi.nlm.nih.gov/pubmed/2777408.
Galvão-Castro B, Loures L, Rodriques LG, Sereno A, Ferreira Júnior OC, Franco LG, et al. Distribution of human T-lymphotropic virus type I among blood donors: a nationwide Brazilian study. Transfusion [Internet]. 1997;37(2):242–3.. Available from: http://www.ncbi.nlm.nih.gov/pubmed/9051104.
Vasquez P, Sanchez G, Volante C, Vera L, Ramirez E, Soto G, et al. Human T-lymphotropic virus type I: new risk for Chilean population. Blood [Internet]. 1991;78(3):850–1.. Available from: http://www.ncbi.nlm.nih.gov/pubmed/1859897.
Bastian I, Hinuma Y, Doherty RR. HTLV-I among Northern Territory aborigines. Med J Aust [Internet]. 1993;159(1):12–6.. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8316104.
Koga Y, Iwanaga M, Soda M, Inokuchi N, Sasaki D, Hasegawa H, et al. Trends in HTLV-1 prevalence and incidence of adult T-cell leukemia/lymphoma in Nagasaki, Japan. J Med Virol [Internet]. 2010;82(4):668–74.. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20166187.
Kaplan JE, Osame M, Kubota H, Igata A, Nishitani H, Maeda Y, et al. The risk of development of HTLV-I-associated myelopathy/tropical spastic paraparesis among persons infected with HTLV-I. J Acquir Immune Defic Syndr [Internet]. 1990;3(11):1096–101.. Available from: http://www.ncbi.nlm.nih.gov/pubmed/2213510.
Mochizuki M, Ono A, Ikeda E, Hikita N, Watanabe T, Yamaguchi K, et al. HTLV-I uveitis. J Acquir Immune Defic Syndr Hum Retrovirol [Internet]. 1996;13(Suppl 1):S50–6.. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8797704.
Pinheiro SRAA, Martins-Filho OA, Ribas JGR, Catalan-Soares BC, Proietti FA, Namen-Lopes S, et al. Immunologic markers, uveitis, and keratoconjunctivitis sicca associated with human T-cell lymphotropic virus type 1. Am J Ophthalmol [Internet]. 2006;142(5):811–5.. Available from: http://www.ncbi.nlm.nih.gov/pubmed/16989761.
Lee R, Schwartz RA. Human T-lymphotropic virus type 1-associated infective dermatitis: a comprehensive review. J Am Acad Dermatol [Internet]. 2011;64(1):152–60.. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20691499.
Pinheiro SR, Lana-Peixoto MA, Proietti AB, Oréfice F, Lima-Martins MV, Proietti FA. HTLV-I-associated uveitis, myelopathy, rheumatoid arthritis and Sjögren’s syndrome. Arq Neuropsiquiatr [Internet]. 1995;53(4):777–81.. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8729772.
Matsuda T, Tomita M, Uchihara J-N, Okudaira T, Ohshiro K, Tomoyose T, et al. Human T-cell leukemia virus type I-infected patients with Hashimoto’s thyroiditis and Graves’ disease. J Clin Endocrinol Metab [Internet]. 2005;90(10):5704–10.. Available from: http://www.ncbi.nlm.nih.gov/pubmed/16076945.
Gabet AS, Mortreux F, Talarmin A, Plumelle Y, Leclercq I, Leroy A, et al. High circulating proviral load with oligoclonal expansion of HTLV-1 bearing T cells in HTLV-1 carriers with strongyloidiasis. Oncogene [Internet]. 2000;19(43):4954–60.. Available from: http://www.ncbi.nlm.nih.gov/pubmed/11042682.
Boxus M, Willems L. Mechanisms of HTLV-1 persistence and transformation. Br J Cancer [Internet]. 2009;101(9):1497–501. Available from: http://www.nature.com/articles/6605345.
Higuchi M, Fujii M. Distinct functions of HTLV-1 Tax1 from HTLV-2 Tax2 contribute key roles to viral pathogenesis. Retrovirology [Internet]. 2009;6:117. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20017952.
Quaresma JAS, Yoshikawa GT, Koyama RVL, Dias GAS, Fujihara S, Fuzii HT. HTLV-1, immune response and autoimmunity. Viruses. 2015;8(1):2–11.
Kibler KV, Jeang KT. CREB/ATF-dependent repression of cyclin a by human T-cell leukemia virus type 1 Tax protein. J Virol [Internet]. 2001;75(5):2161–73. Available from: http://www.ncbi.nlm.nih.gov/pubmed/11160720.
Matsumoto J, Ohshima T, Isono O, Shimotohno K. HTLV-1 HBZ suppresses AP-1 activity by impairing both the DNA-binding ability and the stability of c-Jun protein. Oncogene [Internet]. 2005;24(6):1001–10. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15592508.
Cheng H, Ren T, Sun S. New insight into the oncogenic mechanism of the retroviral oncoprotein Tax. Protein Cell [Internet]. 2012;3(8):581–9. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22865346.
Azran I, Schavinsky-Khrapunsky Y, Aboud M. Role of Tax protein in human T-cell leukemia virus type-I leukemogenicity. Retrovirology [Internet]. 2004;1:20. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15310405.
Satou Y, Yasunaga J, Yoshida M, Matsuoka M. HTLV-I basic leucine zipper factor gene mRNA supports proliferation of adult T-cell leukemia cells. Proc Natl Acad Sci U S A [Internet]. 2006;103(3):720–5. Available from: http://www.ncbi.nlm.nih.gov/pubmed/16407133.
Matsuoka M. Human T-cell leukemia virus type I (HTLV-I) infection and the onset of adult T-cell leukemia (ATL). Retrovirology [Internet]. 2005;2:27. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15854229.
Satou Y, Matsuoka M. HTLV-1 and the host immune system: how the virus disrupts immune regulation, leading to HTLV-1-associated diseases. J Clin Exp Hematop [Internet]. 2010;50(1):1–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20505271.
Hieshima K, Nagakubo D, Nakayama T, Shirakawa A-K, Jin Z, Yoshie O. Tax-inducible production of CC chemokine ligand 22 by human T-cell leukemia virus type 1 (HTLV-1)-infected T cells promotes preferential transmission of HTLV-1 to CCR4-expressing CD4+ T cells. J Immunol [Internet]. 2008;180(2):931–9. Available from: http://www.ncbi.nlm.nih.gov/pubmed/18178833.
Araya N, Sato T, Ando H, Tomaru U, Yoshida M, Coler-Reilly A, et al. HTLV-1 induces a Th1-like state in CD4+CCR4+ T cells. J Clin Invest [Internet]. 2014;124(8):3431–42. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24960164.
Sato T, Coler-Reilly ALG, Yagishita N, Araya N, Inoue E, Furuta R, et al. Mogamulizumab (anti-CCR4) in HTLV-1-associated myelopathy. N Engl J Med [Internet]. 2018;378(6):529–38. Available from: http://www.nejm.org/doi/10.1056/NEJMoa1704827.
Best I, López G, Verdonck K, González E, Tipismana M, Gotuzzo E, et al. IFN-gamma production in response to Tax 161-233, and frequency of CD4+ Foxp3+ and Lin HLA-DRhigh CD123+ cells, discriminate HAM/TSP patients from asymptomatic HTLV-1 carriers in a Peruvian population. Immunology [Internet]. 2009;128(1 Suppl):e777–86. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19740339.
Goncalves DU, Proietti FA, Barbosa-Stancioli EF, Martins ML, Ribas JG, Martins-Filho OA, et al. HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP) inflammatory network. Inflamm Allergy Drug Targets [Internet]. 2008;7(2):98–107. Available from: http://www.ncbi.nlm.nih.gov/pubmed/18691139.
Jia H, Qi H, Gong Z, Yang S, Ren J, Liu Y, et al. The expression of FOXP3 and its role in human cancers. Biochim Biophys Acta Rev Cancer [Internet]. 2019;1871(1):170–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/30630091.
Bacchetta R, Gambineri E, Roncarolo M-G. Role of regulatory T cells and FOXP3 in human diseases. J Allergy Clin Immunol [Internet]. 2007;120(2):227–35; quiz 236–7. Available from: http://www.ncbi.nlm.nih.gov/pubmed/17666212.
Toulza F, Heaps A, Tanaka Y, Taylor GP, Bangham CRM. High frequency of CD4+ FoxP3+ cells in HTLV-1 infection: inverse correlation with HTLV-1-specific CTL response. Blood [Internet]. 2008;111(10):5047–53. Available from: http://www.ncbi.nlm.nih.gov/pubmed/18094326.
Goon PKC, Biancardi A, Fast N, Igakura T, Hanon E, Mosley AJ, et al. Human T-cell lymphotropic virus (HTLV) type-1-specific CD8+ T cells: frequency and immunodominance hierarchy. J Infect Dis [Internet]. 2004;189(12):2294–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15181578.
Jacobson S. Immunopathogenesis of human T-cell lymphotropic virus type I-associated neurologic disease. J Infect Dis [Internet]. 2002;186 Suppl:S187–92. Available from: http://www.ncbi.nlm.nih.gov/pubmed/12424696.
Jeffery KJ, Usuku K, Hall SE, Matsumoto W, Taylor GP, Procter J, et al. HLA alleles determine human T-lymphotropic virus-I (HTLV-I) proviral load and the risk of HTLV-I-associated myelopathy. Proc Natl Acad Sci U S A [Internet]. 1999;96(7):3848–53. Available from: http://www.ncbi.nlm.nih.gov/pubmed/10097126.
Jeffery KJ, Siddiqui AA, Bunce M, Lloyd AL, Vine AM, Witkover AD, et al. The influence of HLA class I alleles and heterozygosity on the outcome of human T-cell lymphotropic virus type I infection. J Immunol [Internet]. 2000;165(12):7278–84. Available from: http://www.ncbi.nlm.nih.gov/pubmed/11120862.
Osame M. Pathological mechanisms of human T-cell lymphotropic virus type I-associated myelopathy (HAM/TSP). J Neurovirol [Internet]. 2002;8(5):359–64. Available from: http://www.ncbi.nlm.nih.gov/pubmed/12402162.
Nagai M, Yamano Y, Brennan MB, Mora CA, Jacobson S. Increased HTLV-I proviral load and preferential expansion of HTLV-I Tax-specific CD8+ T cells in cerebrospinal fluid from patients with HAM/TSP. Ann Neurol [Internet]. 2001;50(6):807–12. Available from: http://www.ncbi.nlm.nih.gov/pubmed/11761481.
Ando H, Sato T, Tomaru U, Yoshida M, Utsunomiya A, Yamauchi J, et al. Positive feedback loop via astrocytes causes chronic inflammation in virus-associated myelopathy. Brain [Internet]. 2013;136(Pt 9):2876–87. Available from: http://www.ncbi.nlm.nih.gov/pubmed/23892452.
Yamano Y, Sato T. Clinical pathophysiology of human T-lymphotropic virus type 1-associated myelopathy/tropical spastic paraparesis. Front Microbiol. 2012;3(NOV):1–10.
Vine AM, Witkover AD, Lloyd AL, Jeffery KJM, Siddiqui A, Marshall SEF, et al. Polygenic control of human T-lymphotropic virus type I (HTLV-I) provirus load and the risk of HTLV-I-associated myelopathy/tropical spastic paraparesis. J Infect Dis [Internet]. 2002;186(7):932–9. Available from: http://www.ncbi.nlm.nih.gov/pubmed/12232833.
Nagai M, Usuku K, Matsumoto W, Kodama D, Takenouchi N, Moritoyo T, et al. Analysis of HTLV-I proviral load in 202 HAM/TSP patients and 243 asymptomatic HTLV-I carriers: high proviral load strongly predisposes to HAM/TSP. J Neurovirol [Internet]. 1998;4(6):586–93. Available from: http://www.ncbi.nlm.nih.gov/pubmed/10065900.
Olindo S, Lézin A, Cabre P, Merle H, Saint-Vil M, Edimonana Kaptue M, et al. HTLV-1 proviral load in peripheral blood mononuclear cells quantified in 100 HAM/TSP patients: a marker of disease progression. J Neurol Sci [Internet]. 2005;237(1–2):53–9. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15972218.
Iwasaki Y. Human T-cell leukemia virus type I infection and chronic myelopathy. Brain Pathol [Internet]. 1993;3(1):1–10. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8269079.
Aye MM, Matsuoka E, Moritoyo T, Umehara F, Suehara M, Hokezu Y, et al. Histopathological analysis of four autopsy cases of HTLV-I-associated myelopathy/tropical spastic paraparesis: inflammatory changes occur simultaneously in the entire central nervous system. Acta Neuropathol [Internet]. 2000;100(3):245–52. Available from: http://www.ncbi.nlm.nih.gov/pubmed/10965793.
Shakudo M, Inoue Y, Tsutada T. HTLV-I-associated myelopathy: acute progression and atypical MR findings. AJNR Am J Neuroradiol [Internet]. 1999;20(8):1417–21. Available from: http://www.ncbi.nlm.nih.gov/pubmed/10512222.
Gadelha SR, Junior Alcântara LC, Costa GC, Acosta AX, Rios D, Kashima S, et al. Correlation between polymorphisms at interleukin-6 but not at interleukin-10 promoter and the risk of human T-lymphotropic virus type I-associated myelopathy/tropical spastic paraparesis in Brazilian individuals. J Med Virol [Internet]. 2008;80(12):2141–6. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19040291.
Treviño A, Vicario JL, Lopez M, Parra P, Benito R, Ortiz de Lejarazu R, et al. Association between HLA alleles and HAM/TSP in individuals infected with HTLV-1. J Neurol [Internet]. 2013;260(10):2551–5. Available from: http://www.ncbi.nlm.nih.gov/pubmed/23835632.
Maloney EM, Cleghorn FR, Morgan OS, Rodgers-Johnson P, Cranston B, Jack N, et al. Incidence of HTLV-I-associated myelopathy/tropical spastic paraparesis (HAM/TSP) in Jamaica and Trinidad. J Acquir Immune Defic Syndr Hum Retrovirol [Internet]. 1998;17(2):167–70. Available from: http://www.ncbi.nlm.nih.gov/pubmed/9473019.
Hisada M, Stuver SO, Okayama A, Li H-C, Sawada T, Hanchard B, et al. Persistent paradox of natural history of human T-lymphotropic virus type I: parallel analyses of Japanese and Jamaican carriers. J Infect Dis [Internet]. 2004;190(9):1605–9. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15478065.
Kaplan JE, Litchfield B, Rouault C, Lairmore MD, Luo CC, Williams L, et al. HTLV-I-associated myelopathy associated with blood transfusion in the United States: epidemiologic and molecular evidence linking donor and recipient. Neurology [Internet]. 1991;41(2 (Pt 1)):192–7. Available from: http://www.ncbi.nlm.nih.gov/pubmed/1992361.
Emmanouilides CE, Territo M. HTLV-I-associated myelopathy following allogeneic bone marrow transplantation. Bone Marrow Transplant [Internet]. 1999;24(2):205–6. Available from: http://www.ncbi.nlm.nih.gov/pubmed/10455351.
Toro C, Rodés B, Poveda E, Soriano V. Rapid development of subacute myelopathy in three organ transplant recipients after transmission of human T-cell lymphotropic virus type I from a single donor. Transplantation [Internet]. 2003;75(1):102–4. Available from: http://www.ncbi.nlm.nih.gov/pubmed/12544880.
Ramos-Remus C, Duran-Barragan S, Castillo-Ortiz JD. Beyond the joints: neurological involvement in rheumatoid arthritis. Clin Rheumatol. 2012;31(1):1–12.
Oliveira P, Castro NM, Muniz AL, Tanajura D, Brandão JC, Porto AF, et al. Prevalence of erectile dysfunction in HTLV-1-infected patients and its association with overactive bladder. Urology [Internet]. 2010;75(5):1100–3. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20189229.
Nakagawa M, Izumo S, Ijichi S, Kubota H, Arimura K, Kawabata M, et al. HTLV-I-associated myelopathy: analysis of 213 patients based on clinical features and laboratory findings. J Neurovirol [Internet]. 1995;1(1):50–61. Available from: http://www.ncbi.nlm.nih.gov/pubmed/9222342.
Gotuzzo E, Cabrera J, Deza L, Verdonck K, Vandamme A-M, Cairampoma R, et al. Clinical characteristics of patients in Peru with human T-cell lymphotropic virus type 1-associated tropical spastic paraparesis. Clin Infect Dis [Internet]. 2004;39(7):939–44. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15472843.
Olindo S, Cabre P, Lézin A, Merle H, Saint-Vil M, Signate A, et al. Natural history of human T-lymphotropic virus 1-associated myelopathy: a 14-year follow-up study. Arch Neurol [Internet]. 2006;63(11):1560–6. Available from: http://www.ncbi.nlm.nih.gov/pubmed/17101824.
Lezin A, Olindo S, Oliere S, Varrin-Doyer M, Marlin R, Cabre P, et al. Human T-lymphotropic virus type I (HTLV-I) proviral load in cerebrospinal fluid: a new criterion for the diagnosis of HTLV-I-associated myelopathy/tropical spastic paraparesis? J Infect Dis [Internet]. 2005;191(11):1830–4. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15871115.
Kirk PD, Witkover A, Courtney A, Lewin AM, Wait R, Stumpf MP, et al. Plasma proteome analysis in HTLV-1-associated myelopathy/tropical spastic paraparesis. Retrovirology [Internet]. 2011;8(1):81. Available from: http://retrovirology.biomedcentral.com/articles/10.1186/1742-4690-8-81.
Morgan DJ, Caskey MF, Abbehusen C, Oliveira-Filho J, Araujo C, Porto AF, et al. Brain magnetic resonance imaging white matter lesions are frequent in HTLV-I carriers and do not discriminate from HAM/TSP. AIDS Res Hum Retroviruses [Internet]. 2007;23(12):1499–504. Available from: http://www.ncbi.nlm.nih.gov/pubmed/18160007.
Griffith C, Bagnato F, Gupta S, Calabrese A, Oh U, Chiu A, et al. Brain volume measurements in patients with human T-cell lymphotropic virus-1-associated tropical spastic paraparesis. J Neurovirol [Internet]. 2006;12(5):349–55. Available from: http://www.ncbi.nlm.nih.gov/pubmed/17065127.
Yukitake M, Takase Y, Nanri Y, Kosugi M, Eriguchi M, Yakushiji Y, et al. Incidence and clinical significances of human T-cell lymphotropic virus type I-associated myelopathy with T2 hyperintensity on spinal magnetic resonance images. Intern Med [Internet]. 2008;47(21):1881–6. Available from: http://www.ncbi.nlm.nih.gov/pubmed/18981631.
De Castro-Costa CM, Araújo AQC, Barreto MM, Takayanagui OM, Sohler MP, ELM DS, et al. Proposal for diagnostic criteria of tropical spastic paraparesis/HTLV-I-associated myelopathy (TSP/HAM). AIDS Res Hum Retroviruses [Internet]. 2006;22(10):931–5. Available from: http://www.liebertonline.com/doi/abs/10.1089/aid.2006.22.931.
Ertzgaard P, Campo C, Calabrese A. Efficacy and safety of oral baclofen in the management of spasticity: a rationale for intrathecal baclofen. J Rehabil Med [Internet]. 2017;49(3):193–203. Available from: http://www.ncbi.nlm.nih.gov/pubmed/28233010.
Lin J, Chay W. Special considerations in assessing and treating spasticity in spinal cord injury. Phys Med Rehabil Clin N Am [Internet]. 2018;29(3):445–53. Available from: http://www.ncbi.nlm.nih.gov/pubmed/30626507.
Moulin D, Boulanger A, Clark AJ, Clarke H, Dao T, Finley GA, et al. Pharmacological management of chronic neuropathic pain: revised consensus statement from the Canadian Pain Society. Pain Res Manag [Internet]. 2014;19(6):328–35. Available from: http://www.ncbi.nlm.nih.gov/pubmed/25479151.
de BVLS, Correa R, Vincent MB. Proprioceptive neuromuscular facilitation in HTLV-I-associated myelopathy/tropical spastic paraparesis. Rev Soc Bras Med Trop [Internet]. 2014;47(1):24–9. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24603733.
Nakagawa M, Nakahara K, Maruyama Y, Kawabata M, Higuchi I, Kubota H, et al. Therapeutic trials in 200 patients with HTLV-I-associated myelopathy/ tropical spastic paraparesis. J Neurovirol [Internet]. 1996;2(5):345–55. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8912211.
Croda MG, de Oliveira ACP, Vergara MPP, Bonasser F, Smid J, Duarte AJ da S, et al. Corticosteroid therapy in TSP/HAM patients: the results from a 10-year open cohort. J Neurol Sci [Internet]. 2008;269(1–2):133–7. Available from: http://www.ncbi.nlm.nih.gov/pubmed/18258264.
Duncan J, Rudge P. Methylprednisolone therapy in tropical spastic paraparesis. J Neurol Neurosurg Psychiatry [Internet]. 1990;53(2):173–4. Available from: http://www.ncbi.nlm.nih.gov/pubmed/2313308.
Taylor GP, Goon P, Furukawa Y, Green H, Barfield A, Mosley A, et al. Zidovudine plus lamivudine in Human T-Lymphotropic Virus type-I-associated myelopathy: a randomized trial. Retrovirology [Internet]. 2006;3:63. Available from: http://www.ncbi.nlm.nih.gov/pubmed/16984654.
Izumo S, Goto I, Itoyama Y, Okajima T, Watanabe S, Kuroda Y, et al. Interferon-alpha is effective in HTLV-I-associated myelopathy: a multicenter, randomized, double-blind, controlled trial. Neurology [Internet]. 1996;46(4):1016–21. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8780082.
Ahmed S, Adonis A, Hilburn S, Demontis M, Fedina A, Haddow J, et al. Treatment of patients with HTLV-1-associated myelopathy with methotrexate. Retrovirology [Internet]. 2014;11(Suppl 1):P33. Available from: http://retrovirology.biomedcentral.com/articles/10.1186/1742-4690-11-S1-P33.
Martin F, Castro H, Gabriel C, Adonis A, Fedina A, Harrison L, et al. Ciclosporin A proof of concept study in patients with active, progressive HTLV-1-associated myelopathy/tropical spastic paraparesis. PLoS Negl Trop Dis [Internet]. 2012;6(6):e1675. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22720101.
Oh U, Yamano Y, Mora CA, Ohayon J, Bagnato F, Butman JA, et al. Interferon-beta1a therapy in human T-lymphotropic virus type I-associated neurologic disease. Ann Neurol [Internet]. 2005;57(4):526–34. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15786444.
Shirabe S, Nakamura T, Tsujino A, Nishiura Y, Furuya T, Goto H, et al. Successful application of pentoxifylline in the treatment of HTLV-I-associated myelopathy. J Neurol Sci [Internet]. 1997;151(1):97–101. Available from: http://www.ncbi.nlm.nih.gov/pubmed/9335018.
Lehky TJ, Fox CH, Koenig S, Levin MC, Flerlage N, Izumo S, et al. Detection of human T-lymphotropic virus type I (HTLV-I) tax RNA in the central nervous system of HTLV-I-associated myelopathy/tropical spastic paraparesis patients by in situ hybridization. Ann Neurol [Internet]. 1995;37(2):167–75. Available from: http://www.ncbi.nlm.nih.gov/pubmed/7847858.
Franzoi AC, Araújo AQC. Disability profile of patients with HTLV-I-associated myelopathy/tropical spastic paraparesis using the Functional Independence Measure (FIM). Spinal Cord [Internet]. 2005;43(4):236–40. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15520834.
Diniz MSC, Feldner PC, Castro RA, Sartori MGF, Girão MJBC. Impact of HTLV-I in quality of life and urogynecologic parameters of women with urinary incontinence. Eur J Obstet Gynecol Reprod Biol [Internet]. 2009;147(2):230–3. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19733955.
Andrade R, Tanajura D, Santana D, dos SD, Carvalho EM. Association between urinary symptoms and quality of life in HTLV-1 infected subjects without myelopathy. Int Braz J Uro [Internet]. 2013;39(6):861–6. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24456778.
Castro NM, Rodrigues W, Freitas DM, Muniz A, Oliveira P, Carvalho EM. Urinary symptoms associated with human T-cell lymphotropic virus type I infection: evidence of urinary manifestations in large group of HTLV-I carriers. Urology [Internet]. 2007;69(5):813–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/17482910.
Netto EC, Brites C. Characteristics of chronic pain and its impact on quality of life of patients with HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP). Clin J Pain [Internet]. 2011;27(2):131–5. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20842011.
Sweet RD. A pattern of eczema in Jamaica. Br J Dermatol [Internet]. 1966;78(2):93–100. Available from: http://www.ncbi.nlm.nih.gov/pubmed/5907441.
LaGrenade L, Hanchard B, Fletcher V, Cranston B, Blattner W. Infective dermatitis of Jamaican children: a marker for HTLV-I infection. Lancet (London, England) [Internet]. 1990;336(8727):1345–7. Available from: http://www.ncbi.nlm.nih.gov/pubmed/1978165.
La Grenade L, Manns A, Fletcher V, Derm D, Carberry C, Hanchard B, et al. Clinical, pathologic, and immunologic features of human T-lymphotropic virus type I-associated infective dermatitis in children. Arch Dermatol [Internet]. 1998;134(4):439–44. Available from: http://www.ncbi.nlm.nih.gov/pubmed/9554295.
Trope BM, Lenzi MER. Infective dermatitis. Clin Dermatol [Internet]. 2009;27(3):281–4. Available from: https://doi.org/10.1016/j.clindermatol.2008.10.007
de Oliveira Mde FSP, Fatal PL, Primo JRL, da Silva JLS, Batista Eda S, Farré L, et al. Infective dermatitis associated with human T-cell lymphotropic virus type 1: evaluation of 42 cases observed in Bahia, Brazil. Clin Infect Dis [Internet]. 2012;54(12):1714–9. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22467669.
LaGrenade L, Sonoda S, Miller W, Pate E, Rodgers-Johnson P, Hanchard B, et al. HLA DRB1∗DQB1∗ haplotype in HTLV-I-associated familial infective dermatitis may predict development of HTLV-I-associated myelopathy/tropical spastic paraparesis. Am J Med Genet [Internet]. 1996;61(1):37–41. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8741915.
Nascimento MCF, Primo J, Bittencourt A, Siqueira I, de Fátima Oliveira M, Meyer R, et al. Infective dermatitis has similar immunological features to human T-lymphotropic virus type 1-associated myelopathy/tropical spastic paraparesis. Clin Exp Immunol [Internet]. 2009;156(3):455–62. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19438598.
Gonçalves DU, Guedes AC, Carneiro-Proietti AB, Lambertucci JR. HTLV-I-associated infective dermatitis may be an indolent HTLV-I associated lymphoma. Braz J Infect Dis [Internet]. 2000;4(2):100–2. Available from: http://www.ncbi.nlm.nih.gov/pubmed/10797656.
Primo JRL, Brites C, de OM d FSP, Moreno-Carvalho O, Machado M, Bittencourt AL. Infective dermatitis and human T-cell lymphotropic virus type 1-associated myelopathy/tropical spastic paraparesis in childhood and adolescence. Clin Infect Dis [Internet]. 2005;41(4):535–41. Available from: http://www.ncbi.nlm.nih.gov/pubmed/16028164.
Bittencourt AL. Adult T-cell leukemia/lymphoma (ATL) in Bahia, Brazil. Brazilian J Infect Dis [Internet]. 2005;9(5):437–8. Available from: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702005000500020&lng=en&nrm=iso&tlng=en.
Maloney EM, Hisada M, Palmer P, Brooks K, Pate E, Wiktor SZ, et al. Human T-cell lymphotropic virus type I-associated infective dermatitis in Jamaica: a case report of clinical and biologic correlates. Pediatr Infect Dis J [Internet]. 2000;19(6):560–5. Available from: http://www.ncbi.nlm.nih.gov/pubmed/10877174.
Van den Hove LE, Van Gool SW, Vandenberghe P, Boogaerts MA, Ceuppens JL. CD57+/CD28- T cells in untreated hemato-oncological patients are expanded and display a Th1-type cytokine secretion profile, ex vivo cytolytic activity and enhanced tendency to apoptosis. Leukemia [Internet]. 1998;12(10):1573–82. Available from: http://www.ncbi.nlm.nih.gov/pubmed/9766502.
Farre L, de Oliveira Mde FP, Primo J, Vandamme A-M, Van Weyenbergh J, Bittencourt AL. Early sequential development of infective dermatitis, human T-cell lymphotropic virus type 1-associated myelopathy, and adult T-cell leukemia/lymphoma. Clin Infect Dis [Internet]. 2008;46(3):440–2. Available from: http://www.ncbi.nlm.nih.gov/pubmed/18173359.
Ohba N, Matsumoto M, Sameshima M, Kabayama Y, Nakao K, Unoki K, et al. Ocular manifestations in patients infected with human T-lymphotropic virus type I. Jpn J Ophthalmol [Internet]. 1989;33(1):1–12. Available from: http://www.ncbi.nlm.nih.gov/pubmed/2733251.
Nakao K, Abematsu N, Sakamoto T. Systemic diseases in patients with HTLV-1-associated uveitis. Br J Ophthalmol [Internet]. 2018;102(3):373–6. Available from: http://bjo.bmj.com/lookup/doi/10.1136/bjophthalmol-2018-312081.
Terada Y, Kamoi K, Komizo T, Miyata K, Mochizuki M. Human T-cell leukemia virus type 1 and eye diseases. J Ocul Pharmacol Ther [Internet]. 2017;33(4):216–23. Available from: http://www.ncbi.nlm.nih.gov/pubmed/28263674.
Ono A, Mochizuki M, Yamaguchi K, Miyata N, Watanabe T. Immunologic and virologic characterization of the primary infiltrating cells in the aqueous humor of human T-cell leukemia virus type-1 uveitis. Accumulation of the human T-cell leukemia virus type-1-infected cells and constitutive expression of viral and. Invest Ophthalmol Vis Sci [Internet]. 1997;38(3):676–89. Available from: http://www.ncbi.nlm.nih.gov/pubmed/9071222.
Merle H, Cabre P, Olindo S, Merle S, Smadja D. Ocular lesions in 200 patients infected by the human T-cell lymphotropic virus type 1 in Martinique (French West Indies). Am J Ophthalmol [Internet]. 2002;134(2):190–5. Available from: http://www.ncbi.nlm.nih.gov/pubmed/12140025.
Taniguchi A, Takenaka Y, Noda Y, Ueno Y, Shichikawa K, Sato K, et al. Adult T-cell leukemia presenting with proliferative synovitis. Arthritis Rheum [Internet]. 1988;31(8):1076–7. Available from: http://www.ncbi.nlm.nih.gov/pubmed/2900640.
Kitajima I, Maruyama I, Maruyama Y, Ijichi S, Eiraku N, Mimura Y, et al. Polyarthritis in human T-lymphotropic virus type I-associated myelopathy. Arthritis Rheum [Internet]. 1989;32(10):1342–4. Available from: http://www.ncbi.nlm.nih.gov/pubmed/2803335.
Hasunuma T, Sumida T, Nishioka K. Human T-cell leukemia virus type-I and rheumatoid arthritis. Int Rev Immunol [Internet]. 1998;17(5–6):291–307. Available from: http://www.ncbi.nlm.nih.gov/pubmed/10036636.
Guérin B, Arfi S, Numéric P, Jean-Baptiste G, Le Parc JM, Smadja D, et al. Polyarthritis in HTLV-1-infected patients. A review of 17 cases. Rev Rhum Engl Ed [Internet]. 1995;62(1):21–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/7788319.
Eguchi K, Origuchi T, Takashima H, Iwata K, Katamine S, Nagataki S. High seroprevalence of anti–HTLV-I antibody in rheumatoid arthritis. Arthritis Rheum [Internet]. 1996;39(3):463–6. Available from: http://doi.wiley.com/10.1002/art.1780390314.
Murphy EL, Wang B, Sacher RA, Fridey J, Smith JW, Nass CC, et al. Respiratory and urinary tract infections, arthritis, and asthma associated with HTLV-I and HTLV-II infection. Emerg Infect Dis [Internet]. 2004;10(1):109–16. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15078605.
Sato K, Maruyama I, Maruyama Y, Kitajima I, Nakajima Y, Higaki M, et al. Arthritis in patients infected with human T-lymphotropic virus type I. Clinical and immunopathologic features. Arthritis Rheum [Internet]. 1991;34(6):714–21. Available from: http://www.ncbi.nlm.nih.gov/pubmed/2053917.
McCallum RM, Patel DD, Moore JO, Haynes BF. Arthritis syndromes associated with human T-cell lymphotropic virus type I infection. Med Clin North Am [Internet]. 1997;81(1):261–76. Available from: http://www.ncbi.nlm.nih.gov/pubmed/9012764.
Nakajima T, Aono H, Hasunuma T, Yamamoto K, Maruyama I, Nosaka T, et al. Overgrowth of human synovial cells driven by the human T-cell leukemia virus type I tax gene. J Clin Invest [Internet]. 1993;92(1):186–93. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8325983.
Sakai M, Eguchi K, Terada K, Nakashima M, Yamashita I, Ida H, et al. Infection of human synovial cells by human T-cell lymphotropic virus type I. Proliferation and granulocyte/macrophage colony-stimulating factor production by synovial cells. J Clin Invest [Internet]. 1993;92(4):1957–66. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8408648.
Yakova M, Lézin A, Dantin F, Lagathu G, Olindo S, Jean-Baptiste G, et al. Increased proviral load in HTLV-1-infected patients with rheumatoid arthritis or connective tissue disease. Retrovirology [Internet]. 2005;2:4. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15686595.
Umekita K, Hidaka T, Miyauchi S, Ueno S, Kubo K, Takajo I, et al. Treatment with anti-tumor necrosis factor biologic agents in human T-lymphotropic virus type I–positive patients with rheumatoid arthritis. Arthritis Care Res (Hoboken) [Internet]. 2014;66(5):788–92. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24127184.
Eguchi K, Matsuoka N, Ida H, Nakashima M, Sakai M, Sakito S, et al. Primary Sjögren’s syndrome with antibodies to HTLV-I: clinical and laboratory features. Ann Rheum Dis [Internet]. 1992;51(6):769–76. Available from: http://www.ncbi.nlm.nih.gov/pubmed/1352097.
Hida A, Kawabe Y, Kawakami A, Migita K, Tominaga M, Nakamura H, et al. HTLV-I-associated Sjögren’s syndrome is aetiologically distinct from anti-centromere antibodies positive Sjögren’s syndrome. Ann Rheum Dis [Internet]. 1999;58(5):320–2. Available from: http://www.ncbi.nlm.nih.gov/pubmed/10225819.
Terada K, Katamine S, Eguchi K, Moriuchi R, Kita M, Shimada H, et al. Prevalence of serum and salivary antibodies to HTLV-1 in Sjögren’s syndrome. Lancet (London, England) [Internet]. 1994;344(8930):1116–9. Available from: http://www.ncbi.nlm.nih.gov/pubmed/7934493.
Gilbert DT, Morgan O, Smikle MF, Simeon D, Barton EN. HTLV-1-associated polymyositis in Jamaica. Acta Neurol Scand [Internet]. 2001;104(2):101–4. Available from: http://www.ncbi.nlm.nih.gov/pubmed/11493227.
Saito M, Higuchi I, Saito A, Izumo S, Usuku K, Bangham CRM, et al. Molecular analysis of T cell clonotypes in muscle-infiltrating lymphocytes from patients with human T-lymphotropic virus type 1 polymyositis. J Infect Dis [Internet]. 2002;186(9):1231–41. Available from: http://www.ncbi.nlm.nih.gov/pubmed/12402192.
Matsuura E, Umehara F, Nose H, Higuchi I, Matsuoka E, Izumi K, et al. Inclusion body myositis associated with human T-lymphotropic virus type I infection: eleven patients from an endemic area in Japan. J Neuropathol Exp Neurol [Internet]. 2008;67(1):41–9. Available from: http://www.ncbi.nlm.nih.gov/pubmed/18091562.
Ozden S, Gessain A, Gout O, Mikol J. Sporadic inclusion body myositis in a patient with human T-cell leukemia virus type 1-associated myelopathy. Clin Infect Dis [Internet]. 2001;32(3):510–4. Available from: http://www.ncbi.nlm.nih.gov/pubmed/11170963.
Smadja D, Bellance R, Cabre P, Arfi S, Vernant JC. Clinical characteristics of HTLV-1-associated dermato-polymyositis. Seven cases from Martinique. Acta Neurol Scand [Internet]. 1995;92(3):206–12. Available from: http://www.ncbi.nlm.nih.gov/pubmed/7484073.
Ozden S, Mouly V, Prevost M-C, Gessain A, Butler-Browne G, Ceccaldi P-E. Muscle wasting induced by HTLV-1 tax-1 protein: an in vitro and in vivo study. Am J Pathol [Internet]. 2005;167(6):1609–19. Available from: http://www.ncbi.nlm.nih.gov/pubmed/16314474.
Higuchi I, Hashimoto K, Matsuoka E, Rosales R, Nakagawa M, Arimura K, et al. The main HTLV-I-harboring cells in the muscles of viral carriers with polymyositis are not macrophages but CD4+ lymphocytes. Acta Neuropathol [Internet]. 1996;92(4):358–61. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8891067.
Ozden S, Cochet M, Mikol J, Teixeira A, Gessain A, Pique C. Direct evidence for a chronic CD8+-T cell-mediated immune reaction to tax within the muscle of a human T-cell leukemia/lymphoma virus type 1-infected patient with sporadic inclusion body myositis. J Virol [Internet]. 2004;78(19):10320–7. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15367598.
Sugimoto M, Nakashima H, Watanabe S, Uyama E, Tanaka F, Ando M, et al. T-lymphocyte alveolitis in HTLV-I-associated myelopathy. Lancet (London, England) [Internet]. 1987;2(8569):1220. Available from: http://www.ncbi.nlm.nih.gov/pubmed/2890850.
Kawabata T, Higashimoto I, Takashima H, Izumo S, Kubota R. Human T-lymphotropic virus type I (HTLV-I)-specific CD8+ cells accumulate in the lungs of patients infected with HTLV-I with pulmonary involvement. J Med Virol [Internet]. 2012;84(7):1120–7. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22585731.
Kikuchi T, Saijo Y, Sakai T, Abe T, Ohnuma K, Tezuka F, et al. Human T-cell lymphotropic virus type I (HTLV-I) carrier with clinical manifestations characteristic of diffuse panbronchiolitis. Intern Med [Internet]. 1996;35(4):305–9. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8739787.
Magno Falcão LF, Falcão ASC, Medeiros Sousa RC, Vieira W de B, de Oliveira RTM, Normando VMF, et al. CT Chest and pulmonary functional changes in patients with HTLV-associated myelopathy in the Eastern Brazilian Amazon. PLoS One [Internet]. 2017;12(11):e0186055. Available from: http://www.ncbi.nlm.nih.gov/pubmed/29095831.
Okada F, Ando Y, Yoshitake S, Yotsumoto S, Matsumoto S, Wakisaka M, et al. Pulmonary CT findings in 320 carriers of human T-lymphotropic virus type 1. Radiology [Internet]. 2006;240(2):559–64. Available from: http://www.ncbi.nlm.nih.gov/pubmed/16864677.
Dias ARN, Falcão LFM, Falcão ASC, Normando VMF, Quaresma JAS. Human T-lymphotropic virus and pulmonary diseases. Front Microbiol. 2018;9(AUG):1–7.
Nakayama Y, Yamazato Y, Tamayose M, Atsumi E, Yara S, Higa F, et al. Increased expression of HBZ and Foxp3 mRNA in bronchoalveolar lavage cells taken from human T-lymphotropic virus type 1-associated lung disorder patients. Intern Med [Internet]. 2013;52(23):2599–609. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24292748.
Desgranges C, Bechet JM, Couderc LJ, Caubarrere I, Vernant JC. Detection of HTLV-1 DNA by polymerase chain reaction in alveolar lymphocytes of patients with tropical spastic paraparesis. J Infect Dis [Internet]. 1989;160(1):162–3. Available from: http://www.ncbi.nlm.nih.gov/pubmed/2732511.
Matsuyama W, Kawabata M, Mizoguchi A, Iwami F, Wakimoto J, Osame M. Influence of human T-lymphotropic virus type I on cryptogenic fibrosing alveolitis - HTLV-I-associated fibrosing alveolitis: proposal of a new clinical entity. Clin Exp Immunol [Internet]. 2003;133(3):397–403. Available from: http://www.ncbi.nlm.nih.gov/pubmed/12930367.
Mori S, Mizoguchi A, Kawabata M, Fukunaga H, Usuku K, Maruyama I, et al. Bronchoalveolar lymphocytosis correlates with human T-lymphotropic virus type I (HTLV-I) proviral DNA load in HTLV-I carriers. Thorax [Internet]. 2005;60(2):138–43. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15681503.
Einsiedel L, Pham H, Wilson K, Walley R, Turpin J, Bangham C, et al. Human T-lymphotropic virus type 1c subtype proviral loads, chronic lung disease and survival in a prospective cohort of Indigenous Australians. PLoS Negl Trop Dis [Internet]. 2018;12(3):e0006281. Available from: http://www.ncbi.nlm.nih.gov/pubmed/29529032.
Bastos Mde L, Santos SB, Souza A, Finkmoore B, Bispo O, Barreto T, et al. Influence of HTLV-1 on the clinical, microbiologic and immunologic presentation of tuberculosis. BMC Infect Dis [Internet]. 2012;12:199. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22925731.
Pedral-Sampaio DB, Martins Netto E, Pedrosa C, Brites C, Duarte M, Harrington WJ. Co-infection of tuberculosis and HIV/HTLV retroviruses: frequency and prognosis among patients admitted in a Brazilian Hospital. Braz J Infect Dis [Internet]. 1997;1(1):31–5. Available from: http://www.ncbi.nlm.nih.gov/pubmed/11107236.
Verdonck K, González E, Schrooten W, Vanham G, Gotuzzo E. HTLV-1 infection is associated with a history of active tuberculosis among family members of HTLV-1-infected patients in Peru. Epidemiol Infect [Internet]. 2008;136(8):1076–83. Available from: http://www.ncbi.nlm.nih.gov/pubmed/17892632.
Shirdel A, Hashemzadeh K, Sahebari M, Rafatpanah H, Hatef M, Rezaieyazdi Z, et al. Is there any association between human lymphotropic virus type I (HTLV-I) infection and systemic lupus erythematosus? an original research and literature review. Iran J Basic Med Sci [Internet]. 2013;16(3):252–7. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24470872.
Sugimoto T, Okamoto M, Koyama T, Takashima H, Saeki M, Kashiwagi A, et al. The occurrence of systemic lupus erythematosus in an asymptomatic carrier of human T-cell lymphotropic virus type I. Clin Rheumatol [Internet]. 2007;26(6):1005–7. Available from: http://www.ncbi.nlm.nih.gov/pubmed/16565895.
Akimoto M, Matsushita K, Suruga Y, Aoki N, Ozaki A, Uozumi K, et al. Clinical manifestations of human T-lymphotropic virus type I-infected patients with systemic lupus erythematosus. J Rheumatol [Internet]. 2007;34(9):1841–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/17696273.
Takayanagui OM, Moura LS, Petean FC, Bíscaro TA, Covas DT, Osame M. Human T-lymphotropic virus type I-associated myelopathy/tropical spastic paraparesis and systemic lupus erythematosus. Neurology [Internet]. 1997;48(5):1469–70. Available from: http://www.ncbi.nlm.nih.gov/pubmed/9153500.
Miura T, Tanaka H, Makino Y, Okamoto K, Iida T, Komura K, et al. Human T-cell leukemia virus type I-associated myelopathy in a patient with systemic lupus erythematosus. Intern Med [Internet]. 1999;38(6):512–5. Available from: http://www.ncbi.nlm.nih.gov/pubmed/10411360.
Ito H, Harada R, Uchida Y, Odashiro K, Uozumi K, Yasumoto Y, et al. Lupus nephritis with adult T-cell leukemia. Nephron [Internet]. 1990;55(3):325–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/2370934.
Bowness P, Davies KA, Tosswill J, Bunn CC, MacAlpine L, Weber JN, et al. Autoimmune disease and HTLV-1 infection. Br J Rheumatol [Internet]. 1991;30(2):141–3. Available from: http://www.ncbi.nlm.nih.gov/pubmed/2012945.
Mizuki M, Tagawa S, Shibano M, Okamoto Y, Nojima J, Sakata K, et al. A HTLV-I carrier who showed various symptoms and antibodies of autoimmune diseases. Intern Med [Internet]. 1993;32(6):449–54. Available from: http://www.ncbi.nlm.nih.gov/pubmed/7902142.
Matsumoto Y, Muramatsu MO, Sato K. Mixed connective tissue disease and Sjögren’s syndrome, accompanied by HTLV-I infection. Intern Med [Internet]. 1993;32(3):261–4. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8101109.
Shimojima Y, Ishii W, Hineno A, Yamamoto K, Matsuda M, Ikeda S. Mixed connective tissue disease with interstitial pneumonia in HTLV-1 carrier: case report and review of the literature. Clin Rheumatol [Internet]. 2004;23(6):548–51. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15278743.
Deguchi HE, Amemiya T. Two cases of uveitis with tubulointerstitial nephritis in HTLV-1 carriers. Jpn J Ophthalmol [Internet]. 2003;47(4):372–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/12842206.
Imasawa T, Kitamura H, Nishimura M, Kawaguchi T, Takata K, Yoshino T, et al. Lupus nephritis class I accompanied by tubulointerstitial nephritis with marked T-lymphocyte infiltration in an HTLV-1-positive patient. CEN Case Reports [Internet]. 2013;2(1):90–7. Available from: http://www.ncbi.nlm.nih.gov/pubmed/28509223.
Nagami S, Konisi T, Kataoka H, Kikui S, Takayanagi T, Suzumura A. [A case with HTLV-I-associated myelopathy (HAM) accompanied by primary biliary cirrhosis (PBC) and autoimmune hepatitis (AIH)]. Rinsho Shinkeigaku [Internet]. 1999;39(11):1132–4. Available from: http://www.ncbi.nlm.nih.gov/pubmed/10689935.
Kawai H, Inui T, Kashiwagi S, Tsuchihashi T, Masuda K, Kondo A, et al. HTLV-I infection in patients with autoimmune thyroiditis (Hashimoto’s thyroiditis). J Med Virol [Internet]. 1992;38(2):138–41. Available from: http://www.ncbi.nlm.nih.gov/pubmed/1460458.
Mizokami T, Okamura K, Ikenoue H, Sato K, Kuroda T, Maeda Y, et al. A high prevalence of human T-lymphotropic virus type I carriers in patients with antithyroid antibodies. Thyroid [Internet]. 1994;4(4):415–9. Available from: http://www.ncbi.nlm.nih.gov/pubmed/7711504.
Kubonishi I, Kubota T, Sawada T, Tanaka Y, Machida H, Yoshida O, et al. An HTLV-I carrier with Graves’ disease followed by uveitis: isolation of HTLV-I from thyroid tissue. Int J Hematol [Internet]. 1997;66(2):233–7. Available from: http://www.ncbi.nlm.nih.gov/pubmed/9277055.
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2019 Springer Nature Switzerland AG
About this chapter
Cite this chapter
Fuentes, A., Burgos, P.I. (2019). HTLV-1: A View from the Rheumatologist. In: Espinoza, L. (eds) Infections and the Rheumatic Diseases. Springer, Cham. https://doi.org/10.1007/978-3-030-23311-2_16
Download citation
DOI: https://doi.org/10.1007/978-3-030-23311-2_16
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-030-23310-5
Online ISBN: 978-3-030-23311-2
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)