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Adjunctive interleukin-2 for the treatment of drug-susceptible tuberculosis: a randomized control trial in China

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Abstract

Purpose

Evaluation of the efficacy and safety of IL-2 in the treatment of drug-susceptible tuberculosis.

Methods

First, the cases of diagnosed drug-susceptible tuberculosis were randomized into two groups—the control group that received the background regimen of isoniazid, rifampin, pyrazinamide, and ethambutol, and the experimental group that received the background regimen plus IL-2. The efficacy and safety evaluations were performed throughout the therapy process as well as 12 months after the treatment completion.

Results

A total of 1151 patients underwent the randomization, among which 539 (96.2%) of the 560 in the experimental group achieved the sputum culture conversion to negative, compared to the 551 (93.2%) of the 591 in the control group, after 2 months of treatment, with significant difference observed between the groups (P = 0.025). Cavity closure after 2 months in the IL-2 (experimental) group was 60/211 (28.4%) compared to 46/248 (18.5%) in the control group, with a significant difference between the groups (P = 0.001). After treatment completion, the proportion of favorable outcomes was 559/560 (99.8%) in the experimental group and 587/591 (99.3%) in the control group, with no significant difference between the groups. Twelve months after treatment completion, relapse occurred in 15/560 (2.6%) in the IL-2 group and 19/591 (3.2%) in the control group, with no significant difference.

Conclusion

IL-2 may enhance culture conversion and the cavity closure rate in the early treatment phase, although the enhancement may not be significant after treatment completion.

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Data availability

The data sets used or analysed during the current study are available from the corresponding author on reasonable request.

Code availability

Not applicable.

References

  1. Fauci AS. Multidrug-resistant and extensively drug-resistant tuberculosis: the National Institute of Allergy and Infectious Diseases Research agenda and recommendations for priority research. J Infect Dis. 2008;197:1493.

    Article  Google Scholar 

  2. Matteelli A, Migliori GB, Cirillo D, Centis R, Girard E, Raviglion M. Multidrug-resistant and extensively drug-resistant Mycobacterium tuberculosis: epidemiology and control. Expert Rev Anti Infect Ther. 2007;5:857–971.

    Article  CAS  Google Scholar 

  3. Giedlin MA, Zimmerman RJ. The use of recombinant human interleukin-2 in treating infectious diseases. Curr Opin Biotechnol. 1993;4:722–6.

    Article  CAS  Google Scholar 

  4. Scott P. IFN-gamma modulates the early development of Th1 and Th2 responses in a murine model of cutaneous leishmaniasis. J lmmunol. 1991;147:3149–55.

    CAS  Google Scholar 

  5. Morgan DA, Ruscetti FW, Gallo R. Selective in vitro growth of T lymphocytes from normal human bone marrows. Science. 1976;193:1007–8.

    Article  CAS  Google Scholar 

  6. Lin JX, Leonard WJ. The role of Stat5a and Stat5b in signaling by IL-2 family cytokines. Oncogene. 2000;19:2566–76.

    Article  CAS  Google Scholar 

  7. Malek TR, Castro I. Interleukin-2 receptor signaling: at the interface between tolerance and immunity. Immunity. 2010;33:153–265.

    Article  CAS  Google Scholar 

  8. Boyman O, Sprent J. The role of interleukin-2 during homeostasis and activation of the immune system. Nat Rev Immunol. 2012;12:180–90.

    Article  CAS  Google Scholar 

  9. Mosman TR. Two types of murine helper T cell clone. I. Definition according to profiles of lymphokine activities and secreted proteins. J Immunol. 1986;136:2348–57.

    Google Scholar 

  10. Rc REES. The Biological Response to Interleukin-2. In: Waxman J, Balkwill F, editors. lnterleukin-2. Oxford: Blackwell Scientific Publications; 1992. p. 47–8.

    Google Scholar 

  11. Bermudez LE, Young LS. Tumor necrosis factor, alone or incombination with IL-2, but not IFN-gamma, is associated with macrophage killing of Mycobacterium avium complex. J Immunol. 1988;140:3006–13.

    CAS  PubMed  Google Scholar 

  12. Bermudez LE, Stevens P, Kolonoski P, Wu M, Young LS. Treatment of experimental disseminated Mycobacterium avium complex infection in mice with recombinant IL-2 and tumor necrosis factor. J Immunol. 1989;143:2996–3000.

    CAS  PubMed  Google Scholar 

  13. Jeevan A, Asherson GL. Recombinant interleukin-2 limits the replication of Mycobacterium lepraemurium and Mycobacterium bovis BCG in mice. Lymphokine Res. 1988;7:129–40.

    CAS  PubMed  Google Scholar 

  14. Akuffo H, Kaplan G, Kiessling R, Teklemariam S, Dietz M, McElrath J, et al. Administration of recombinant interleukin-2 reduces the local parasite load of patients with disseminated cutaneous leishmaniasis. J Infect Dis. 1990;161:775–80.

    Article  CAS  Google Scholar 

  15. Converse P, Ottenhoff TH, Work Teklemariam S, Hancock GE, Dietz M, Becx-Bleumink M, et al. Intradermal recombinant interleukin 2 enhances peripheral blood T-cell responses to mitogen and antigens in patients with lepromatous leprosy. Scand J Immunol. 1990;32:83–91.

    Article  CAS  Google Scholar 

  16. Hancock GE, Molloy A, Ab BK, Kiessling R, Becx-Bleumink M, Cohn ZA, et al. In vivo administration of low-dose human interleukin-2 induces lymphokine-activated killer cells for enhanced cytolysis in vitro. Cell Immunol. 1991;132:277–84.

    Article  CAS  Google Scholar 

  17. Hancock GE, Cohn ZA, Kaplan G. The generation of antigen-specific, major histocompatibility complex-restricted cytotoxic T lymphocytes of the CD4+ phenotype: enhancement by the cutaneous administration of interleukin 2. J Exp Med. 1989;169:909–19.

    Article  CAS  Google Scholar 

  18. Kaplan G, Kiessling R, Teklemariam S, Hancock G, Sheftel G, Job CK, et al. The reconstitution of cell-mediated immunity in the cutaneous lesions of lepromatous leprosy by recombinant interleukin 2. J Exp Med. 1989;169:893–907.

    Article  CAS  Google Scholar 

  19. Kaplan G, Britton WJ, Hancock GE, Theuvenet WJ, Smith KA, Job CK, et al. The systemic influence of recombinant interleukin 2 on the manifestations of lepromatous leprosy. J Exp Med. 1991;173:993–1006.

    Article  CAS  Google Scholar 

  20. Johnson BJ, Ress SR, Willcox P, Pati BP, Lorgat F, Stead P, et al. Clinical and immune responses of tuberculosis patients treated with low-dose IL-2 and multidrug therapy. Cytokines Mol Ther. 1995;1:185–96.

    CAS  PubMed  Google Scholar 

  21. Johnson BJ, Bekker LG, Rickman R, Brown S, Lesser M, Ress S, et al. rhuIL-2 adjunctive therapy in multidrug resistant tuberculosis: a comparison of two treatment regimens and placebo. Tuber Lung Dis. 1997;78:195–203.

    Article  CAS  Google Scholar 

  22. Johnson JL, Ssekasanvu E, Okwera A, Mayanja H, Hirsch CS, Nakibali JG, et al. Randomized trial of adjunctive interleukin-2 in adults with pulmonary tuberculosis. Respir Crit Care Med. 2003;168:185–91.

    Article  Google Scholar 

  23. Treatment of tuberculosis: guidelines for national programmes. 2010. WHO. Geniva.

  24. Tan Q, Min R, Dai GQ, Wang YL, Nan L, Yang Z, et al. Clinical and immunological effects of rhIL-2 therapy in Eastern Chinese patients with multidrug-resistant tuberculosis. Sci Rep. 2017;7:17854.

    Article  Google Scholar 

  25. Chu NH, Zhu LZ, Yie ZZ, Yuan SL, Wang JY, Xu JL, et al. A controlled clinical study on the efficacy of recombinant human interleukin-2 in the treatment of pulmonary tuberculosis. Zhonghua Jie He He Hu Xi Za Zhi. 2003;26:548–51.

    PubMed  Google Scholar 

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Funding

This research was funded by 12th and 13th Five National Major Scientific and Technological Projects [2017ZX09304009 and 2015ZX10003001-002].

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Authors and Affiliations

Authors

Contributions

WN protocol design and paper writing; JW and JZ: laboratory operating; QW, YD, QT, WX, QD, GD, XL, ZL, JZ, JP, KL, LC, HD, CZ, QJ, XC, JC, NW, YC, CQ, AD, PR, YL, CL, SC, HL, HY: sample selecting; NC protocol reviewing and paper revising.

Corresponding author

Correspondence to Naihui Chu.

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Conflict of interest

None.

Ethical approval

The protocol of the present study was approved by the ethics committee of the Beijing Chest Hospital affiliated with the Capital Medical University.

Consent to participate

Not applicable.

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Yes.

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Nie, W., Wang, J., Zeng, J. et al. Adjunctive interleukin-2 for the treatment of drug-susceptible tuberculosis: a randomized control trial in China. Infection 50, 413–421 (2022). https://doi.org/10.1007/s15010-021-01698-3

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  • DOI: https://doi.org/10.1007/s15010-021-01698-3

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