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Mucosal signatures of pathogenic T cells in HLA-B*27+ anterior uveitis and axial spondyloarthritis
Michael A. Paley, Xinbo Yang, Lynn M. Hassman, Frank Penkava, Lee I. Garner, Grace L. Paley, Nicole Linskey, Ryan Agnew, Paulo Henrique Arantes de Faria, Annie Feng, Sophia Y. Li, Davide Simone, Elisha D.O. Roberson, Philip A. Ruzycki, Ekaterina Esaulova, Jennifer Laurent, Lacey Feigl-Lenzen, Luke E. Springer, Chang Liu, Geraldine M. Gillespie, Paul Bowness, K. Christopher Garcia, Wayne M. Yokoyama
Michael A. Paley, Xinbo Yang, Lynn M. Hassman, Frank Penkava, Lee I. Garner, Grace L. Paley, Nicole Linskey, Ryan Agnew, Paulo Henrique Arantes de Faria, Annie Feng, Sophia Y. Li, Davide Simone, Elisha D.O. Roberson, Philip A. Ruzycki, Ekaterina Esaulova, Jennifer Laurent, Lacey Feigl-Lenzen, Luke E. Springer, Chang Liu, Geraldine M. Gillespie, Paul Bowness, K. Christopher Garcia, Wayne M. Yokoyama
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Research Article

Mucosal signatures of pathogenic T cells in HLA-B*27+ anterior uveitis and axial spondyloarthritis

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Abstract

HLA-B*27 was one of the first HLA alleles associated with an autoimmune disease, i.e., axial spondyloarthritis (axSpA) and acute anterior uveitis (B27AAU), which cause joint and eye inflammation, respectively. Gastrointestinal inflammation has been suggested as a trigger of axSpA. We recently identified a bacterial peptide (YeiH) that can be presented by HLA-B*27 to expanded public T cell receptors in the joint in axSpA and the eye in B27AAU. While YeiH is present in enteric microbiota and pathogens, additional evidence that pathogenic T cells in HLA-B*27–associated autoimmunity may have had a prior antigenic encounter within the gastrointestinal tract remains lacking. Here, we analyzed ocular, synovial, and blood T cells in B27AAU and axSpA, showing that YeiH-specific CD8+ T cells express a mucosal gene set and surface proteins consistent with intestinal differentiation, including CD161, integrin α4β7, and CCR6. In addition, we found an expansion of YeiH-specific CD8+ T cells in axSpA and B27AAU blood compared with that from individuals acting as healthy controls, whereas influenza-specific CD8+ T cells were equivalent across groups. Finally, we demonstrated the dispensability of TRBV9 for antigen recognition. Collectively, our data suggest that, in HLA-B27–associated autoimmunity, early antigen exposure and differentiation of pathogenic CD8+ T cells may occur in enteric organs.

Authors

Michael A. Paley, Xinbo Yang, Lynn M. Hassman, Frank Penkava, Lee I. Garner, Grace L. Paley, Nicole Linskey, Ryan Agnew, Paulo Henrique Arantes de Faria, Annie Feng, Sophia Y. Li, Davide Simone, Elisha D.O. Roberson, Philip A. Ruzycki, Ekaterina Esaulova, Jennifer Laurent, Lacey Feigl-Lenzen, Luke E. Springer, Chang Liu, Geraldine M. Gillespie, Paul Bowness, K. Christopher Garcia, Wayne M. Yokoyama

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Figure 4

YeiH.232-240–specific CD8+ T cells express markers of enteric trafficking and differentiation.

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YeiH.232-240–specific CD8+ T cells express markers of enteric traffickin...
(A) Identification of HLA-B*27(YeiH.232-240)+ and HLA-B*27(NP.383-391)+ CD8+ T cells by flow cytometry in the peripheral blood of a participant with B27AAU. Cells are gated on CD4–CD19–Va7.2–Va24.Ja18–CD3+CD8+ T cells. (B) Quantification of HLA-B*27(YeiH.232-240)+ CD8+ T cells in peripheral blood from HLA-B*27+ individuals acting as healthy controls (n = 10) and participants with HLA*B27+ axSpA and/or B27AAU (n = 31). Tetramer+ cells are shown both as a percentage of all CD8+ T cells as well as the number of cells per 1 million PBMCs. (C) Quantification of HLA-B*27(NP.383-391)+ CD8+ T cells in the same groups as in B. (D) Expression of CD161, integrin α4β7, CCR6, CD103, and CD28 on HLA-B*27(YeiH.232-240)+ (red), HLA-B*27(NP.383-391)+ (blue), and tetramer– (black) CD8+ T cells in participants with B27AAU and/or axSpA. (E) Quantification of D (n = 14). *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001, Mann-Whitney test (B and C) or 2-way ANOVA with Dunnett’s multiple comparisons test (E).

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