Heterologous Cytomegalovirus and Allo-Reactivity by Shared T Cell Receptor Repertoire in Kidney Transplantation
Jazyk angličtina Země Švýcarsko Médium electronic-ecollection
Typ dokumentu klinické zkoušky, časopisecké články, pozorovací studie, práce podpořená grantem
PubMed
31736968
PubMed Central
PMC6834532
DOI
10.3389/fimmu.2019.02549
Knihovny.cz E-zdroje
- Klíčová slova
- ELISPOT, TCR repertoire, cross-reactivity, cytomegalovirus, heterologous immunity, kidney transplantation, rejection,
- MeSH
- alografty MeSH
- biopsie MeSH
- cytomegalovirové infekce * etiologie genetika imunologie patologie MeSH
- Cytomegalovirus imunologie MeSH
- dospělí MeSH
- imunologická paměť * MeSH
- isoantigeny genetika imunologie MeSH
- kohortové studie MeSH
- lidé středního věku MeSH
- lidé MeSH
- receptory antigenů T-buněk alfa-beta * imunologie MeSH
- T-lymfocyty * mikrobiologie patologie MeSH
- transplantace ledvin * MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky MeSH
- pozorovací studie MeSH
- práce podpořená grantem MeSH
- Názvy látek
- isoantigeny MeSH
- receptory antigenů T-buněk alfa-beta * MeSH
Cytomegalovirus (CMV) infection is associated with allograft rejection but the mechanisms behind are poorly defined yet. Although cross-reactivity of T cells to alloantigen and CMV has been hypothesized, direct evidence in patients is lacking. In this observational cohort study, we tested the pre-transplant effector/memory T cell response to CMV peptide pools and alloantigen in 78 living donor/recipient pairs using the interferon-gamma Enzyme-Linked ImmunoSpot (ELISPOT) assay. To prove the hypothesis of cross-reactivity, we analyzed by applying next-generation sequencing the T cell receptor ß (TCR- ß) repertoire of CMV- and alloantigen-reactive T cells enriched from peripheral pre-transplant blood of 11 CMV-seropositive and HLA class I mismatched patients. Moreover, the TCR-repertoire was also analyzed in the allograft biopsies of those patients. There was a significant association between the presence of pre-transplant CMV immediate-early protein 1 (IE-1)-specific effector/memory T cells and acute renal allograft rejection and function (p = 0.01). Most importantly, we revealed shared TCR-ß sequences between CMV-IE1 and donor alloantigen-reactive T cells in all pre-transplant peripheral blood samples analyzed in CMV-seropositive patients who received HLA class I mismatched grafts. Identical TCR sequences were also found in particular in post-transplant allograft biopsies of patients with concomitant CMV infection and rejection. Our data show the presence of functional, cross-reactive T cells and their clonotypes in peripheral blood and in kidney allograft tissue. It is therefore likely that CMV-donor cross-reactivity as well as CMV specific T cell elicited inflammation is involved in the processes that affect allograft outcomes.
Department of Immunogenetics Institute for Clinical and Experimental Medicine Prague Czechia
Department of Transplant Surgery Institute for Clinical and Experimental Medicine Prague Czechia
Transplant Laboratory Institute for Clinical and Experimental Medicine Prague Czechia
Zobrazit více v PubMed
Reinke P, Prosch S, Kern F, Volk HD. Mechanisms of human cytomegalovirus (HCMV) (re)activation and its impact on organ transplant patients. Transpl Infect Dis. (1999) 1:157–64. 10.1034/j.1399-3062.1999.010304.x PubMed DOI
Rafailidis PI, Mourtzoukou EG, Varbobitis IC, Falagas ME. Severe cytomegalovirus infection in apparently immunocompetent patients: a systematic review. Virol J. (2008) 5:47. 10.1186/1743-422X-5-47 PubMed DOI PMC
Klenerman P, Oxenius A. T cell responses to cytomegalovirus. Nat Rev Immunol. (2016) 16:367–77. 10.1038/nri.2016.38 PubMed DOI
Reinke P, Fietze E, Ode-Hakim S, Prosch S, Lippert J, Ewert R, et al. . Late-acute renal allograft rejection and symptomless cytomegalovirus infection. Lancet. (1994) 344:1737–8. 10.1016/S0140-6736(94)92887-8 PubMed DOI
Cainelli F, Vento S. Infections and solid organ transplant rejection: a cause-and-effect relationship? Lancet Infect Dis. (2002) 2:539–49. 10.1016/S1473-3099(02)00370-5 PubMed DOI
Sharma S, Thomas PG. The two faces of heterologous immunity: protection or immunopathology. J Leukoc Biol. (2014) 95:405–16. 10.1189/jlb.0713386 PubMed DOI PMC
Gamadia LE, Remmerswaal EB, Surachno S, Lardy NM, Wertheim-van Dillen PM, van Lier RA, et al. . Cross-reactivity of cytomegalovirus-specific CD8+ T cells to allo-major histocompatibility complex class I molecules. Transplantation. (2004) 77:1879–85. 10.1097/01.TP.0000131158.81346.64 PubMed DOI
Heutinck KM, Yong SL, Tonneijck L, van den Heuvel H, van der Weerd NC, van der Pant KA, et al. Virus-specific CD8(+) T cells cross-reactive to donor-alloantigen are transiently present in the circulation of kidney transplant recipients infected with CMV and/or EBV. Am J Transplant. (2016) 16:1480–91. 10.1111/ajt.13618 PubMed DOI
Kim SK, Brehm MA, Welsh RM, Selin LK. Dynamics of memory T cell proliferation under conditions of heterologous immunity and bystander stimulation. J Immunol. (2002) 169:90–8. 10.4049/jimmunol.169.1.90 PubMed DOI
Yin Y, Mariuzza RA. The multiple mechanisms of T cell receptor cross-reactivity. Immunity. (2009) 31:849–51. 10.1016/j.immuni.2009.12.002 PubMed DOI
van den Heuvel H, Heutinck KM, van der Meer-Prins EP, Yong SL, Claas FH, Ten Berge IJ. Detection of virus-specific CD8+ T cells with cross-reactivity against alloantigens: potency and flaws of present experimental methods. Transplant Direct. (2015) 1:e40. 10.1097/TXD.0000000000000550 PubMed DOI PMC
D'Orsogna L, van den Heuvel H, van Kooten C, Heidt S, Claas FHJ. Infectious pathogens may trigger specific allo-HLA reactivity via multiple mechanisms. Immunogenetics. (2017) 69:631–41. 10.1007/s00251-017-0989-3 PubMed DOI PMC
Viklicky O, Hribova P, Volk HD, Slatinska J, Petrasek J, Bandur S, et al. . Molecular phenotypes of acute rejection predict kidney graft prognosis. J Am Soc Nephrol. (2010) 21:173–80. 10.1681/ASN.2008121268 PubMed DOI PMC
Nickel P, Bold G, Presber F, Biti D, Babel N, Kreutzer S, et al. . High levels of CMV-IE-1-specific memory T cells are associated with less alloimmunity and improved renal allograft function. Transpl Immunol. (2009) 20:238–42. 10.1016/j.trim.2008.11.002 PubMed DOI
Bestard O, Lucia M, Crespo E, Van Liempt B, Palacio D, Melilli E, et al. . Pretransplant immediately early-1-specific T cell responses provide protection for CMV infection after kidney transplantation. Am J Transplant. (2013) 13:1793–805. 10.1111/ajt.12256 PubMed DOI
Gebauer BS, Hricik DE, Atallah A, Bryan K, Riley J, Tary-Lehmann M, et al. . Evolution of the enzyme-linked immunosorbent spot assay for post-transplant alloreactivity as a potentially useful immune monitoring tool. Am J Transplant. (2002) 2:857–66. 10.1034/j.1600-6143.2002.20908.x PubMed DOI
Tanaka N, Kimura H, Iida K, Saito Y, Tsuge I, Yoshimi A, et al. . Quantitative analysis of cytomegalovirus load using a real-time PCR assay. J Med Virol. (2000) 60:455–62. 10.1002/(SICI)1096-9071(200004)60:4<455::AID-JMV14>3.0.CO;2-Q PubMed DOI
Hubacek P, Virgili A, Ward KN, Pohlreich D, Keslova P, Goldova B, et al. . HHV-6 DNA throughout the tissues of two stem cell transplant patients with chromosomally integrated HHV-6 and fatal CMV pneumonitis. Br J Haematol. (2009) 145:394–8. 10.1111/j.1365-2141.2009.07622.x PubMed DOI
Kotrova M, Muzikova K, Mejstrikova E, Novakova M, Bakardjieva-Mihaylova V, Fiser K, et al. . The predictive strength of next-generation sequencing MRD detection for relapse compared with current methods in childhood ALL. Blood. (2015) 126:1045–7. 10.1182/blood-2015-07-655159 PubMed DOI PMC
Theunissen P, Mejstrikova E, Sedek L, van der Sluijs-Gelling AJ, Gaipa G, Bartels M, et al. . Standardized flow cytometry for highly sensitive MRD measurements in B-cell acute lymphoblastic leukemia. Blood. (2017) 129:347–57. 10.1182/blood-2016-07-726307 PubMed DOI PMC
van Dongen JJ, Langerak AW, Bruggemann M, Evans PA, Hummel M, Lavender FL, et al. . Design and standardization of PCR primers and protocols for detection of clonal immunoglobulin and T-cell receptor gene recombinations in suspect lymphoproliferations: report of the BIOMED-2 concerted action BMH4-CT98–3936. Leukemia. (2003) 17:2257–317. 10.1038/sj.leu.2403202 PubMed DOI
Duez M, Giraud M, Herbert R, Rocher T, Salson M, Thonier F. Vidjil: A web platform for analysis of high-throughput repertoire sequencing. PLoS ONE. (2016) 11:e0166126. 10.1371/journal.pone.0166126 PubMed DOI PMC
Crespo E, Lucia M, Cruzado JM, Luque S, Melilli E, Manonelles A, et al. Pre-transplant donor-specific T-cell alloreactivity is strongly associated with early acute cellular rejection in kidney transplant recipients not receiving T-cell depleting induction therapy. PLoS ONE. (2015) 10:e0117618 10.1371/journal.pone.0117618 PubMed DOI PMC
Hricik DE. Transplant immunology and immunosuppression: core curriculum 2015. Am J Kidney Dis. (2015) 65:956–66. 10.1053/j.ajkd.2015.01.026 PubMed DOI
Slezak SL, Bettinotti M, Selleri S, Adams S, Marincola FM, Stroncek DF. CMV pp65 and IE-1 T cell epitopes recognized by healthy subjects. J Transl Med. (2007) 5:17. 10.1186/1479-5876-5-17 PubMed DOI PMC
Selvey LA, Lim WH, Boan P, Swaminathan R, Slimings C, Harrison AE, et al. . Cytomegalovirus viraemia and mortality in renal transplant recipients in the era of antiviral prophylaxis. Lessons from the western Australian experience. BMC Infect Dis. (2017) 17:501. 10.1186/s12879-017-2599-y PubMed DOI PMC
Fisher RA. Cytomegalovirus infection and disease in the new era of immunosuppression following solid organ transplantation. Transpl Infect Dis. (2009) 11:195–202. 10.1111/j.1399-3062.2009.00372.x PubMed DOI
Humar A, Lebranchu Y, Vincenti F, Blumberg EA, Punch JD, Limaye AP, et al. . The efficacy and safety of 200 days valganciclovir cytomegalovirus prophylaxis in high-risk kidney transplant recipients. Am J Transplant. (2010) 10:1228–37. 10.1111/j.1600-6143.2010.03074.x PubMed DOI
Reischig T, Hribova P, Jindra P, Hes O, Bouda M, Treska V, et al. . Long-term outcomes of pre-emptive valganciclovir compared with valacyclovir prophylaxis for prevention of cytomegalovirus in renal transplantation. J Am Soc Nephrol. (2012) 23:1588–97. 10.1681/ASN.2012010100 PubMed DOI PMC
Sylwester AW, Mitchell BL, Edgar JB, Taormina C, Pelte C, Ruchti F, et al. . Broadly targeted human cytomegalovirus-specific CD4+ and CD8+ T cells dominate the memory compartments of exposed subjects. J Exp Med. (2005) 202:673–85. 10.1084/jem.20050882 PubMed DOI PMC
Ford ML. Virally-induced heterologous immunity in renal transplant recipients: important or inconsequential? Am J Transplant. (2016) 16:1348–9. 10.1111/ajt.13657 PubMed DOI PMC
Kern F, Faulhaber N, Frommel C, Khatamzas E, Prosch S, Schonemann C, et al. . Analysis of CD8 T cell reactivity to cytomegalovirus using protein-spanning pools of overlapping pentadecapeptides. Eur J Immunol. (2000) 30:1676–82. 10.1002/1521-4141(200006)30:6<1676::AID-IMMU1676>3.0.CO;2-V PubMed DOI
Prosch S, Staak K, Stein J, Liebenthal C, Stamminger T, Volk HD, et al. . Stimulation of the human cytomegalovirus IE enhancer/promoter in HL-60 cells by TNFalpha is mediated via induction of NF-kappaB. Virology. (1995) 208:197–206. 10.1006/viro.1995.1143 PubMed DOI
Zeng G, Huang Y, Huang Y, Lyu Z, Lesniak D, Randhawa P. Antigen-specificity of T cell infiltrates in biopsies with T cell-mediated rejection and BK polyomavirus viremia: analysis by next generation sequencing. Am J Transplant. (2016) 16:3131–8. 10.1111/ajt.13911 PubMed DOI PMC
Amir AL, D'Orsogna LJ, Roelen DL, van Loenen MM, Hagedoorn RS, de Boer R, et al. . Allo-HLA reactivity of virus-specific memory T cells is common. Blood. (2010) 115:3146–57. 10.1182/blood-2009-07-234906 PubMed DOI
D'Orsogna LJ, Roelen DL, van der Meer-Prins EM, van der Pol P, Franke-van Dijk ME, Eikmans M, et al. . Tissue specificity of cross-reactive allogeneic responses by EBV EBNA3A-specific memory T cells. Transplantation. (2011) 91:494–500. 10.1097/TP.0b013e318207944c PubMed DOI
Jackson SE, Sedikides GX, Okecha G, Poole EL, Sinclair JH, Wills MR. Latent Cytomegalovirus (CMV) infection does not detrimentally alter T cell responses in the healthy old, but increased latent CMV carriage is related to expanded CMV-specific T cells. Front Immunol. (2017) 8:733. 10.3389/fimmu.2017.00733 PubMed DOI PMC