Abstract
Inflammatory bowel disease (IBD) occurring following allogeneic stem cell transplantation (aSCT) is a very rare condition. The underlying pathogenesis needs to be better defined. There is currently no systematic effort to exclude loss- or gain-of-function mutations in immune-related genes in stem cell donors. This is despite the fact that more than 100 inborn errors of immunity may cause or contribute to IBD. We have molecularly characterized a patient who developed fulminant inflammatory bowel disease following aSCT with stable 100% donor-derived hematopoiesis. A pathogenic c.A291G; p.I97M HAVCR2 mutation encoding the immune checkpoint protein TIM-3 was identified in the patient’s blood-derived DNA, while being absent in DNA derived from the skin. TIM-3 expression was much decreased in the patient’s serum, and in vitro-activated patient-derived T cells expressed reduced TIM-3 levels. In contrast, T cell-intrinsic CD25 expression and production of inflammatory cytokines were preserved. TIM-3 expression was barely detectable in the immune cells of the patient’s intestinal mucosa, while being detected unambiguously in the inflamed and non-inflamed colon from unrelated individuals. In conclusion, we report the first case of acquired, “transplanted” insufficiency of the regulatory TIM-3 checkpoint linked to post-aSCT IBD.
Similar content being viewed by others
Avoid common mistakes on your manuscript.
Introduction
Inborn errors of immunity (IEI) are a large group of genetically determined diseases caused by germline loss- or gain-of-function mutations in immune-related genes. More than 480 IEI entities have been described to date [1]. More than 100 of those can be associated with IBD [2, 3]. The clinical penetrance of IEI-related mutations is often low to moderate [4]. However, immune-dysregulating post-transplant events, such as lymphopenia, treatment with immune-regulating drugs or infections might increase the clinical penetrance [4, 5]. In addition, environmental factors, such as the herbizide propyzamide, contribute to IBD pathogenesis [6]. The clinical phenotype of IEI is often broad and may even vary within carriers of the exact same variant in a family [7, 8].
The occurrence of inflammatory bowel disease (IBD) in non-IEI patients after allogeneic stem cell transplantation for hematological malignancies is extremely rare [9,10,11,12,13]. No molecular explanation has yet been uncovered in these rare cases. Allogeneic stem cell transplantation (aSCT) can be curative for patients with hematological malignancies and even represents a potentially beneficial treatment option for severe treatment-refractory Crohn’s disease [14]. Post aSCT, patients can develop graft-versus-host disease (GvHD) affecting various organs, including the gut, which is caused by donor-derived T cell-mediated inflammation [15]. Histological findings of GvHD of the small bowel and colon are characterized by crypt epithelial cell apoptosis and segmental crypt loss or fibrosis of the submucosa, with or without a dense lymphocytic infiltrate [16]. By contrast, the pathogenesis of a post-aSCT IBD remains unclear. Since aSCT donors are currently not genetically screened for carriage of rare IEI variants, there is a non-neglectable risk of transferring risk alleles potentially modifying post-transplant immune health in general and post-aSCT IBD in particular.
Methods
Consent
The prospective cohort study of the functional and genetic architecture of patients with primary immune dysregulation (FuGe-PID) has been approved by the ethics commission of Northwestern Switzerland (EKNZ215-187).
Flow Cytometric Analysis of T Cells and In Vitro Stimulation of Peripheral Blood Mononuclear Cells (PBMC)
Lymphocyte flow cytometric phenotyping of peripheral blood depicted in Supplemental Table 1 was performed as part of the routine immunology laboratory diagnostics of the Basel University Hospital as described [17]. Peripheral blood mononuclear cells (PBMCs) were isolated by standard density-gradient centrifugation (Lymphoprep, Fresenius Kabi). For detection of TIM-3 expression, freshly isolated PBMCs were adjusted to a concentration of 2 × 106/ml and stimulated with 5 µg/ml phytohemagglutinin (Sigma-Aldrich) and 0.325 IE/ml IL-2 (Novartis). Immune cell populations and Tim-3 expression were identified by staining with fluorophore-conjugated anti-CD4, anti-CD8, anti-CD25, and anti-Tim-3 vs. mouse IgG1 κ isotype control (all BioLegend) at 4 °C for 30 min. For detection of cytokine production, flat bottom plates were coated overnight at 4 °C with 1 µg/ml agonistic anti-CD3 (OKT3, BioLegend) and 2 µg/ml agonistic anti-CD28 (CD28.2, BioLegend). Freshly isolated PBMCs were adjusted to 2 × 106/ml and incubated for 4 h on the previously coated plate in the presence of Brefeldin A (BioLegend). Cytokine expression was identified by staining with fluorophore-conjugated anti-CD3, anti-CD4, anti-CD8, anti-IFNG, anti-IL17, and anti-CD69 (all BioLegend). Fluorescence data was acquired using CytoFLEX (Beckman Coulter) cytometers and BD LSR Fortessa (BD Biosciences). Cell populations and median fluorescence intensities (MFI) were determined using FlowJo (BD Biosciences, formerly developed by FlowJo LLC). In vitro stimulated PBMC as described above were additionally cultured in the absence of Brefeldin A, and 4 h later, cell pellets were stored in RNA lysis buffer to analyze cytokine mRNA production. A full description of the used antibodies is provided in Supplemental Methods.
Flowcytometric Assessment of Monocytes
1.5 × 106 PBMC were stained for 30 min at 4 °C using antibodies against CD163 (BV421, clone GHI/61), CCR2 (BV510, clone K036C2), CD14 (BV605, clone MSE2), CD16 (APC-Fire750, clone 3G8), CD11b (BV711, clone ICRF44), HLA-DR (A488, clone L243), CD45 (PerCpCy5.5, clone HI30), CD209 (PE, clone 9E9A8), CD19 (PECy5, clone HIB19), CD3 (PECy5, clone UCHT1), CD56 (PECy5, clone 5.1H11), CD20 (PECy5, clone 2H7), TCRb (PECy5, clone UP26), and Fc block (clone FC1). All antibodies were purchased from BioLegend, except for Fc block which was obtained from BD Biosciences. Cell analysis was performed on a FACS LSRII Fortessa (BD Biosciences). Acquired data were analyzed using FlowJo software (Version 10.8.1, BD Biosciences).
RNA Isolation, cDNA Generation, and Real-Time PCR Analysis
RNA isolation was performed using a QIAamp RNA blood mini kit according to the manufacturer’s protocol (Qiagen). Before reverse transcription, RNA was digested with DNAse I Amplification Grade Kit (Sigma) at 37 °C for 30 min. Afterwards, DNAse was inactivated at 65 °C for 10 min. Next, random primers (Promega) were annealed at 70 °C for 5 min, and cDNA was synthesized by GoTaq G2 DNA Polymerase (Promega) in a TProfessional TRIO PCR Thermocycler (Core Life Sciences) according to the manufacturer’s protocol. cDNA levels were assessed by quantitative PCR in a qPCR cycler ABI machine (Applied Biosystems, Thermo Fisher Scientific) using a Sybr Green method according to the manufacturer’s protocol (Promega). As reference genes for normalization, we used 18 s rRNA, Actin, and IPO8. For every gene, the mean expression of all control samples was set to 100%, and each individual sample was normalized to this (% of control).
Whole Exome Sequencing and Targeted Sanger Sequencing
Whole exome sequencing and bioinformatics were performed as recently described [17].
Peripheral blood or skin-derived genomic DNA of the index patient was isolated using the QIAamp® DNA Mini kit (Qiagen) according to the manufacturer’s protocol. DNA was amplified by polymerase chain reaction (PCR). All primers used were designed by Primer-BLAST and are listed in Supplemental Methods.
End-point PCR was performed using the GoTaq G2 DNA Polymerase (Promega) according to the manufacturer’s protocol with a primer concentration of 0.5 µM. PCR was performed on a TProfessional TRIO PCR Thermocycler (Core Life Sciences). PCR products were separated and visualized on a 1.5% agarose gel. Specific bands were cut and purified using the Qiagen Gel Extraction kit. Sanger sequencing was performed by the company Microsynth.
To generate complementary DNA (cDNA) of the index patient, RNA was isolated using the QIAamp® RNA Blood Mini Kit (QIAGEN) according to the manufacturer’s protocol. RNA concentration was determined using the NanoDrop 2000c (Thermo Fischer Scientific). DNA was digested with the DNase I Amplification Grade Kit (Sigma-Aldrich). Random primers (Promega) were annealed at 70 °C for 5 min. cDNA synthesis was performed according to the Qiagen’s GoScript Reverse Transcription System protocol in a TProfessional TRIO PCR Thermocycler (Core Life Sciences).
Real-Time PCR Analysis of Inflammatory Cytokine Expression
RNA isolation was performed using a QIAamp RNA blood mini kit according to the manufacturer’s protocol (Qiagen). Prior to reverse transcription, RNA was digested with DNAse I Amplification Grade Kit (Sigma) at 37 °C for 30 min. Afterwards, DNAse was inactivated at 65 °C for 10 min. Next, random primers (Promega) were annealed at 70 °C for 5 min, and cDNA was synthesized by GoTaq G2 DNA Polymerase (Promega) in a TProfessional TRIO PCR Thermocycler (Core Life Sciences) according to the manufacturer’s protocol. The freshly synthesized cDNA was examined by quantitative PCR in a qPCR cycler ABI machine (Applied Biosystems, Thermo Fischer Scientific) using a Sybr Green method according to the Manufacturer’s protocol (Promega). As reference genes for normalization, we used 18 s rRNA, ACTB (actin), and IPO8. Afterwards, we calculated the mean of all controls and applied it to each individual sample to calculate the percent change compared to the norm. Primers used are listed in Supplemental Methods.
Pathology Studies and Immunohistology
A TIM-3 specific monoclonal antibody (clone D5D5R, Cell Signaling, Danvers, MA, USA) was used to detect TIM-3 in immune histology. A CD5-specific monoclonal antibody (clone SP19, Ventana/Roche, Tucson, AZ, USA) was used to stain mucosal T cells in general. FOXP3 was stained with an antibody from ABCAM (clone SP97), and ROR-γt was stained with an antibody from Biocare Medical (clone 6F3.1).
Quantification of Serum TIM-3 and Galectin-9 Levels by ELISA
Serum TIM-3 and Galectin-9 levels were determined by ELISA kits as recently reported [18] in multiple sera from the index patient (patient) over a period of 6 years (2017–2023), sera from healthy controls (control), and sera from randomly assigned patients enrolled into our prospective immune-dysregulation cohort (disease control).
Chimerism Analysis in Sorted Lymphocyte and Monocyte Populations
For chimerism analysis, we took advantage of the sex mismatch between patient (male) and donor (female) and used a diagnostically validated, highly sensitive (limit of detection, LoD 0.01%) digital PCR-based approach to specifically amplify the SRY gene sequence on the Y chromosome. CD3+CD4+ vs. CD3+CD8+ T cells and CD56+CD3− NK cells of the index patient were flow cytometrically sorted, and monocytes were enriched by using a monocyte rosette separation kit (STEMCELL Technologies).
Results
A currently 50-year-old male patient was treated with a 10/10 HLA allele-matched, unrelated, and sex-mismatched (female donor) allogeneic stem cell transplantation (aSCT) in August 2012 due to a T cell prolymphocytic leukemia. The clinical status of the stem cell donor was requested from the bone marrow registry, and well-being had been documented at the last 5 years after the transplant. A conditioning regimen with the BEAM-Fludarabine 2Gy total body irradiation protocol (carmustine, etoposide, cytarabine, melphalan, and fludarabin) was applied in combination with anti-thymocyte globulin (ATG) to reduce the recurrence of malignant T cells. The post-transplant course was complicated by acute graft-versus-host disease (GvHD, overall stage 3) of the skin (stage 3), liver (stage 2), and intestine (stage 1) occurring 2 weeks after aSCT. Acute GvHD which was well-controlled by steroids (which were subsequently tapered) and single administration of 10 mg alemtuzumab (anti-CD52). Exacerbation of skin GvHD was documented in September 2013, followed by reinforced immune suppression with systemic steroids and extracorporeal photopheresis for 6 months followed by treatment with the Janus kinase (JAK) inhibitor ruxolitinib. At the regular visit 2 years after transplantation in September 2014, chronic GvHD was overall scored moderate with stomatitis (stage 1), and skin GvHD (stage 2). GvHD-targeting immune-suppressive treatment could eventually be stopped. At the time of writing, only very mild chronic GvHD (skin stage 1, oral stage 1) was documented. Since aSCT, chimerism analysis in myeloid cells and lymphocytes has been repeatedly performed as part of the routine clinical follow-up, always demonstrating 100% donor chimerism (last analysis in 2019). In November 2023, we further sorted CD4+ vs. CD8+ T cells vs. NK cells vs. monocytes of the patient and demonstrated 100% donor chimerism in all these immune cell subpopulations using a highly sensitive droplet-based PCR analysis (data not shown, see Methods).
Five years after aSCT, the patient presented with watery diarrhea. After stool multiplex-PCR ruled out bacterial, viral, or parasite pathogens, colonoscopy revealed a moderate left-sided colitis, histologically associated with non-specific inflammation but neither evidence of cytomegalovirus (CMV) infection nor GvHD (Lerner grade 0). Broad-spectrum antibiotics and short-term budesonide were associated with transient improvement. However, within a few weeks, the patient developed bloody diarrhea and abdominal cramps. Blood tests revealed leukocytosis, markedly elevated C-reactive protein, and a newly developed iron deficiency anemia. Stool calprotectin was > 800 ug/g stool, pathogen multiplex stool-PCR screening, including Clostridioides difficile, was negative, and the computer tomography (CT)-imaging demonstrated a severe pancolitis. A repeat colonoscopy confirmed an erosive pancolitis and a moderate terminal ileitis (Supplemental Fig. 1). Histologically, multiple crypt abscesses, distortion of the crypt architecture on colonic biopsies, and an erosive inflammation with cryptitis in the ileum were consistent with diagnosis of Crohn’s disease (CD) (Supplemental Fig. 1). No evidence of GvHD or CMV infection was found. Gastro-duodenoscopy performed at this time showed the absence of duodenal inflammation and no evidence of Whipple’s disease. High-dose prednisolone therapy with a tapering scheme, along with an infliximab induction therapy (5 mg/kg body weight), was initiated. The patient achieved remission which was maintained clinically, biochemically, and endoscopically up to the present with infliximab every 6–8 weeks in the absence of steroids. In this stable remission, the distribution of lymphocyte and T cell subpopulations in peripheral blood was analyzed, demonstrating normal T cell numbers with a preserved CD4+/CD8+ T cell ratio > 1. CD25hiCD127lo regulatory CD4 T cell frequencies were also normal, naïve CD4 T cells were slightly low, and follicular T helper cells were relatively elevated compared to age- and sex-matched reference values (Table 1).
Since the development of CD after aSCT is a very rare observation at our center and sparsely reported in the literature, we prepared genomic DNA from the patient’s blood and skin to search for rare immune gene variants linked to inborn errors of immunity (IEI)—a group of genetically determined immune system diseases often manifesting with gastrointestinal inflammation. Whole exome and Sanger sequencing of the blood-derived DNA detected a rare missense variant (c.A291G; p.I97M; rs35960726; allele frequency based on the gnomAD database: 0.002885) in the HAVCR2 gene, which encodes for the immune-regulatory protein TIM-3 (Fig. 1a). In contrast to TIM-3 insufficiency associated with germline HAVCR2 mutations [19, 20], our patient did carry the mutation specifically in hematopoietic cells as it was absent in skin-derived DNA (Fig. 1a). Whole exome sequencing data did not reveal additional disease-causing mutations in genes linked to IEI as listed in the most recent report by the International Union of Immunology Societies expert group [1]. We, however, cannot exclude that additional rare variants in IEI genes may have contributed to the clinical phenotype [21].
To measure whether the heterozygous HAVCR2 mutation leads to reduced TIM-3 expression in immune cells, we in vitro stimulated patient-derived T cells with PHA/IL-2 for 48 h and measured TIM-3 expression by flow cytometry. Analysis of TIM-3 expression in stimulated T cells from a total of eleven unrelated healthy volunteers served as a control. Patient-derived T cells upregulated CD25 normally, while TIM-3 expression was approximately 20% of normal in CD4+ T cells (Fig. 1b, c). Reduced TIM-3 expression in the patient was a stable trait as it was measured on four occasions over a time span of more than 2.5 years (Fig. 1c). HAVCR2 mRNA levels in non-stimulated PBMCs of the patient were lower compared to controls (Fig. 1d), arguing for enhanced RNA decay of the mutated HAVCR2 allele. Stably reduced soluble TIM-3 levels [22] (sTIM-3) were measured by ELISA in the serum of the index patient using sera over a time course of 6 years (Fig. 1e). This was contrasted by elevated Galectin-9 levels in the patient’s serum, suggesting a negative feedback loop (Fig. 1e) similar to what has been described for other immune-regulating signaling pathways [23]. As myeloid cells have been demonstrated to be functionally shaped by TIM-3 [24], we additionally flow cytometrically phenotyped peripheral monocytes of the patient without detecting abnormal subset distribution (Fig. 2a). We further assessed patient-derived T cells ex vivo and following in vitro stimulation but did not find differences vs. controls with regards to expression of FOXP3 (Fig. 2b) or the levels of IFN-γ, IL-17A, and IL-2 (Fig. 2d). Notably, CCR6+CCR4+ T cells, which are linked to the Th17 lineage, were higher in the patient than observed in controls (Fig. 2c).
The immune histology of patient-derived intestinal biopsies was performed to examine TIM-3 expression in T cells within intestinal tissue. While CD5+ T cells were easily detectable in the patient’s stomach, duodenum, ileum, and colon, TIM-3 positive lymphocytes were almost completely absent, independent of the IBD activity (Fig. 3, Supplemental Fig. 2). In contrast, TIM-3 positive lymphocytes were present in both inflamed and non-inflamed colon from unrelated individuals (Fig. 3). Control stainings revealed the presence of FOXP3 and ROR-γ positive cells predominantly in the inflamed colon of the patient and controls (Supplemental Figs. 3 and 4).
Discussion
The c.A291G; p.I97M HAVCR2/TIM-3 mutation has been demonstrated to encode a loss of function allele and has, in homozygous but also in heterozygous states, been shown to cause subcutaneous panniculitis-like T cell lymphoma (SPTCL) and autoinflammatory disease [19]. Also, cases of autoinflammation in the absence of SPTCL have been recently linked to HAVCR2 germline mutations [25, 26]. The I97M missense mutation causes TIM-3 misfolding, aggregation in the Golgi apparatus, and lack of surface expression [19]. In addition, our results suggest enhanced RNA decay of the mutated HAVCR2 allele. It has been previously reported that heterozygous HAVCR2 mutations, including the I97M found here, can be associated with TIM-3 insufficiency [19, 20]. In fact, a careful review of the immune-histological and clinical features of patients with heterozygous TIM-3 mutations did not reveal differences from patients with homozygous mutations [20]. The molecular reason for this is currently unknown but is supported by our own data showing TIM-3 expression around 20% of normal in CD4+ T cells associated with heterozygous carriage of the p.I97M missense mutation. Our patient’s HAVCR2 mutation was donor-derived since donor chimerism was 100%. There was no overt immunologic disease reported in the stem cell donor. Potential stem cell donors undergo extensive health check-ups; however, there is currently no standard screening for IEI- or hematologic malignancy-related mutations [27, 28]. The clinical penetrance of disease associated with TIM-3 missense mutations, especially in heterozygous state, has, to our knowledge, not been studied. The clinical penetrance of IEI gene mutations in general is often rather low and is known to be influenced by environmental, genetic, and epigenetic factors [4]. TIM-3 expression is enhanced in ex vivo analyzed CD4+ T cells of the intestinal mucosa compared to the peripheral blood [29]. TIM-3 down-regulation has been described during human IBD flares [29, 30], and blockade of TIM-3 function exacerbates inflammation in murine colitis models [24, 31]. Vice versa, the TIM-3 ligand Galectin-9 has been recently demonstrated to reduce 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced colitis in mice [32]. Homozygous carriage of the TIM-3 Thr101Ile missense variant (rs147827860, not the same variant as detected in our patient) has been linked to human IBD [33]. These results are corroborated by recent genome-wide association studies demonstrating the linkage of TIM-3 mutations and CD [34]. Accordingly, insufficient expression of other regulatory immune checkpoint molecules, such as CTLA-4 [35, 36], or inactivation of their regulatory function by checkpoint inhibitors [37] can cause colitis. Thus, the link between TIM-3 deficiency and human IBD appears plausible.
Conclusion
This is the first description of an acquired, hematopoietic cell-intrinsic, pathogenic HAVCR2 mutation associated with TIM-3 deficiency in blood-derived and intestinal immune cells clinically linked with post-aSCT IBD.
Data Availability
The data underlying this article will be shared on reasonable request to the corresponding authors.
References
Tangye SG, Al-Herz W, Bousfiha A, Cunningham-Rundles C, Franco JL, Holland SM, et al. Human inborn errors of immunity: 2022 update on the classification from the International Union of Immunological Societies Expert Committee. J Clin Immunol. 2022;42(7):1508–20. https://doi.org/10.1007/s10875-022-01352-z.
Bolton C, Smillie CS, Pandey S, Elmentaite R, Wei G, Argmann C, et al. An integrated taxonomy for monogenic inflammatory bowel disease. Gastroenterology. 2022;162(3):859–76.
Sazonovs A, Stevens CR, Venkataraman GR, Yuan K, Avila B, Abreu MT, et al. Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility. Nat Genet. 2022;54(9):1275–83.
Gruber C, Bogunovic D. Incomplete penetrance in primary immunodeficiency: a skeleton in the closet. Hum Genet. 2020;139(6–7):745–57.
King C, Ilic A, Koelsch K, Sarvetnick N. Homeostatic expansion of T cells during immune insufficiency generates autoimmunity. Cell. 2004;117(2):265–77.
Sanmarco LM, Chao CC, Wang YC, Kenison JE, Li Z, Rone JM, et al. Identification of environmental factors that promote intestinal inflammation. Nature. 2022.
Delmonte OM, Schuetz C, Notarangelo LD. RAG deficiency: two genes, many diseases. J Clin Immunol. 2018;38(6):646–55.
Pilania RK, Banday AZ, Sharma S, Kumrah R, Joshi V, Loganathan S, et al. Deficiency of human adenosine deaminase type 2 - a diagnostic conundrum for the hematologist. Front Immunol. 2022;13:869570.
Spiers AS. Ulcerative colitis after bone-marrow transplantation for acute leukemia. N Engl J Med. 1984;311(19):1259.
Baron FA, Hermanne JP, Dowlati A, Weber T, Thiry A, Fassotte MF, et al. Bronchiolitis obliterans organizing pneumonia and ulcerative colitis after allogeneic bone marrow transplantation. Bone Marrow Transplant. 1998;21(9):951–4.
Sonwalkar SA, James RM, Ahmad T, Zhang L, Verbeke CS, Barnard DL, et al. Fulminant Crohn’s colitis after allogeneic stem cell transplantation. Gut. 2003;52(10):1518–21.
Boussen I, Sokol H, Aractingi S, Georges O, Hoyeau-Idrissi N, Hugot JP, et al. Inflammatory bowel disease after allogeneic stem cell transplantation. Bone Marrow Transplant. 2015;50(10):1365–6.
Onaka T, Kitagawa T, Mori M, Yonezawa A, Imada K. Infliximab therapy for Crohn’s-like gastrointestinal lesions after allogeneic bone marrow transplantation. Rinsho Ketsueki. 2015;56(12):2452–5.
Brierley CK, Castilla-Llorente C, Labopin M, Badoglio M, Rovira M, Ricart E, et al. Autologous Haematopoietic stem cell transplantation for Crohn’s disease: a retrospective survey of long-term outcomes from the European Society for Blood and Marrow Transplantation. J Crohns Colitis. 2018;12(9):1097–103.
Zeiser R, Blazar BR. Acute graft-versus-host disease - biologic process, prevention, and therapy. N Engl J Med. 2017;377(22):2167–79.
Wong NA, Marks DI. How many serial sections are needed to detect apoptosis in endoscopic biopsies with gastrointestinal graft versus host disease? J Clin Pathol. 2020;73(6):358–60.
Burgener AV, Bantug GR, Meyer BJ, Higgins R, Ghosh A, Bignucolo O, et al. SDHA gain-of-function engages inflammatory mitochondrial retrograde signaling via KEAP1-Nrf2. Nat Immunol. 2019;20(10):1311–21.
Konantz M, Williams M, Merkel T, Reiss A, Dirnhofer S, Meyer SC, et al. Increased TIM-3 and galectin-9 serum levels in patients with advanced systemic mastocytosis. J Allergy Clin Immunol. 2023;152(4):1019–24.
Gayden T, Sepulveda FE, Khuong-Quang DA, Pratt J, Valera ET, Garrigue A, et al. Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome. Nat Genet. 2018;50(12):1650–7.
Koh J, Jang I, Mun S, Lee C, Cha HJ, Oh YH, et al. Genetic profiles of subcutaneous panniculitis-like T-cell lymphoma and clinicopathological impact of HAVCR2 mutations. Blood Adv. 2021;5(20):3919–30.
Meyer BJ, Kunz N, Seki S, Higgins R, Ghosh A, Hupfer R, et al. Immunologic and genetic contributors to CD46-dependent immune dysregulation. J Clin Immunol. 2023;43(8):1840–56. https://doi.org/10.1007/s10875-023-01547-y.
Bailly C, Thuru X, Goossens L, Goossens JF. Soluble TIM-3 as a biomarker of progression and therapeutic response in cancers and other of human diseases. Biochem Pharmacol. 2023;209:115445.
Berger CT, Rebholz-Chaves B, Recher M, Manigold T, Daikeler T. Serial IL-6 measurements in patients with tocilizumab-treated large-vessel vasculitis detect infections and may predict early relapses. Ann Rheum Dis. 2019;78(7):1012–4.
Jiang X, Yu J, Shi Q, Xiao Y, Wang W, Chen G, et al. Tim-3 promotes intestinal homeostasis in DSS colitis by inhibiting M1 polarization of macrophages. Clin Immunol. 2015;160(2):328–35.
Tromp SAM, Gillissen MA, Bernelot Moens SJ, van Leeuwen EMM, Jansen MH, Koens L, et al. Treatment of an HLH-mimic disease based on HAVCR2 variants with absent TIM-3 expression. Blood Adv. 2022;6(15):4501–5.
Tada M, Kachi S, Onozawa M, Fujieda Y, Yoshida S, Oki Y, et al. Subcutaneous panniculitis-like T-cell lymphoma lacking subcutaneous tumor mimicking adult-onset Still’s disease. Intern Med. 2023;62(21):3231–5. https://doi.org/10.2169/internalmedicine.1419-22.
Williams LS, Williams KM, Gillis N, Bolton K, Damm F, Deuitch NT, et al. Donor-derived malignancy and transplantation morbidity: risks of patient and donor genetics in allogeneic hematopoietic stem cell transplantation. Transplant Cell Ther. 2023;S2666–6367(23):01640–8. https://doi.org/10.1016/j.jtct.2023.10.018.
Gurnari C, Robin M, Godley LA, Drozd-Sokolowska J, Wlodarski MW, Raj K, et al. Germline predisposition traits in allogeneic hematopoietic stem-cell transplantation for myelodysplastic syndromes: a survey-based study and position paper on behalf of the Chronic Malignancies Working Party of the EBMT. Lancet Haematol. 2023;10(12):e994–1005.
Morimoto K, Hosomi S, Yamagami H, Watanabe K, Kamata N, Sogawa M, et al. Dysregulated upregulation of T-cell immunoglobulin and mucin domain-3 on mucosal T helper 1 cells in patients with Crohn’s disease. Scand J Gastroenterol. 2011;46(6):701–9.
Kim MJ, Lee WY, Choe YH. Expression of TIM-3, human beta-defensin-2, and FOXP3 and correlation with disease activity in pediatric Crohn’s disease with infliximab therapy. Gut Liver. 2015;9(3):370–80.
Li X, Chen G, Li Y, Wang R, Wang L, Lin Z, et al. Involvement of T cell Ig mucin-3 (Tim-3) in the negative regulation of inflammatory bowel disease. Clin Immunol. 2010;134(2):169–77.
Xiong H, Xue G, Zhang Y, Wu S, Zhao Q, Zhao R, et al. Effect of exogenous galectin-9, a natural TIM-3 ligand, on the severity of TNBS- and DSS-induced colitis in mice. Int Immunopharmacol. 2023;115:109645.
Huang YH, Zhu C, Kondo Y, Anderson AC, Gandhi A, Russell A, et al. CEACAM1 regulates TIM-3-mediated tolerance and exhaustion. Nature. 2015;517(7534):386–90.
Lin D, Zhu RC, Tang C, Li FF, Gao ML, Wang YQ. Association of TIM-3 with anterior uveitis and associated systemic immune diseases: a Mendelian randomization analysis. Front Med. 2023;10:1183326 (Lausanne).
Schwab C, Gabrysch A, Olbrich P, Patino V, Warnatz K, Wolff D, et al. Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjects. J Allergy Clin Immunol. 2018;142(6):1932–46.
Joosse ME, Nederlof I, Walker LSK, Samsom JN. Tipping the balance: inhibitory checkpoints in intestinal homeostasis. Mucosal Immunol. 2019;12(1):21–35.
Tang L, Wang J, Lin N, Zhou Y, He W, Liu J, et al. Immune checkpoint inhibitor-associated colitis: from mechanism to management. Front Immunol. 2021;12:800879.
Acknowledgements
We thank the patient for his continuing support of this study. We thank the clinical staff for detailed and provident clinical care.
Funding
Open access funding provided by University of Basel This work was supported by the Swiss National Science Foundation (grant numbers: PP00P3_181038 and 310030_192652) to Mike Recher. Karin Hartmann is supported by the following grants: Swiss National Science Foundation (grant 310030_207705), Swiss Cancer Research Foundation (grant KFS-5979-08-2023), and EU-H2020-MSCA-COFUND EURIdoc programme (No. 101034170).
Author information
Authors and Affiliations
Contributions
MR and PH: conception and supervision of the study and writing of the manuscript. AB and DA: acquisition of most clinical and translational data. TM: performed immune histology and contributed to article writing. BD, SG, JP, and JH: acquisition of data and critical revision of the manuscript reg. allogenic stem cell transplant. DJ: chimerism analysis of sorted immune cell populations. CMB and IH: data acquisition of immune-phenotyping and critical revision of the manuscript. AG, FP, and KP: analysis of next-generation sequencing data. JH, RH, JK, BM, and AJ: data acquisition. IP and CC: provided material and critically read the manuscript. KD, TD, CH, CTB, and JHN: critical revision of the manuscript. MK and KH: quantification of serum TIM-3 and Galectin-9 levels. AN and CH: contributed to study design and critical revision of the manuscript. HY: critical revision of the manuscript and data acquisition.
Corresponding authors
Ethics declarations
Ethics Approval
The prospective cohort study of the functional and genetic architecture of patients with primary immune dysregulation (FuGe-PID) has been approved by the ethics commission of Northwestern Switzerland (EKNZ215-187).
Consent to Participate
Informed consent was obtained from all individual participants included in the study.
Consent for Publication
The authors affirm that human research participants provided informed consent for the publication of the endoscopy and histology images.
Competing Interests
The authors declare no competing interests.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
This work has not been published previously and is not under consideration elsewhere.
Adrian Baldrich and Dominic Althaus are shared first authors.
Mike Recher and Petr Hruz are shared senior authors.
Supplementary Information
Below is the link to the electronic supplementary material.
10875_2024_1667_MOESM1_ESM.pdf
Supplementary file1 (PDF 2747 KB) Supplemental Figure 1 Representative endoscopic appearance (top) and H+E conventional histology of colon tissue (bottom) of the index patient during active colitis are depicted.
10875_2024_1667_MOESM2_ESM.pdf
Supplementary file2 (PDF 32934 KB) Supplemental Figure 2 Sections of the indicated intestinal tissues of the index patient in clinical remission (under infliximab therapy) were stained by immune-histology for T cells (CD5) and for TIM-3 expression.
10875_2024_1667_MOESM3_ESM.jpg
Supplementary file3 (JPG 4707 KB) Supplemental Figure 3 Sections from the same tissue samples analyzed in Figure 2 were assessed by immune-histology for staining of T cells expressing the transcription factors Foxp3 and ROR-γt.
10875_2024_1667_MOESM4_ESM.jpg
Supplementary file4 (JPG 4381 KB) Supplemental Figure 4 Sections of the indicated intestinal tissues of the index patient in clinical remission under infliximab therapy (same tissues as analyzed in Supplemental Figure 2) were analyzed by immune histology for Foxp3 and ROR-γt expressing T cells.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Baldrich, A., Althaus, D., Menter, T. et al. Post-transplant Inflammatory Bowel Disease Associated with Donor-Derived TIM-3 Deficiency. J Clin Immunol 44, 63 (2024). https://doi.org/10.1007/s10875-024-01667-z
Received:
Accepted:
Published:
DOI: https://doi.org/10.1007/s10875-024-01667-z