Dipeptidyl peptidase 4 (DPP4, CD26) is a serine protease that is expressed constitutively by many haematopoietic and non-haematopoietic tissues. It exists as a membrane-associated protein, as well as in an active, soluble form (herein called sDPP4), present at high concentrations in bodily fluids. Despite the proposed use of sDPP4 as a biomarker for multiple diseases, its cellular sources are not well defined. Here, we report that individuals with congenital lymphocyte immunodeficiency had markedly lower serum concentrations of sDPP4, which were restored upon successful treatment and restoration of lymphocyte haematopoiesis. Using irradiated lymphopenic mice and wild-type to Dpp4–/– reciprocal bone marrow chimeric animals, we found that haematopoietic cells were a major source of circulating sDPP4. Furthermore, activation of human and mouse T lymphocytes resulted in increased sDPP4, providing a mechanistic link between immune system activation and sDPP4 concentration. Finally, we observed that acute viral infection induced a transient increase in sDPP4, which correlated with the expansion of antigen-specific CD8+T cell responses. Our study demonstrates that sDPP4 concentrations are determined by the frequency and activation state of lymphocyte populations. Insights from these studies will support the use of sDPP4 concentration as a biomarker for inflammatory and infectious diseases.

Lymphocytes are a major source of circulating soluble dipeptidyl peptidase 4 / Casrouge, A.; Sauer, A. V.; Barreira Da Silva, R.; Tejera-Alhambra, M.; Sanchez-Ramon, S.; Cancrini, C.; Ingersoll, M. A.; Aiuti, A.; Albert, M. L.. - In: CLINICAL AND EXPERIMENTAL IMMUNOLOGY. - ISSN 0009-9104. - 194:2(2018), pp. 166-179. [10.1111/cei.13163]

Lymphocytes are a major source of circulating soluble dipeptidyl peptidase 4

Aiuti A.;
2018-01-01

Abstract

Dipeptidyl peptidase 4 (DPP4, CD26) is a serine protease that is expressed constitutively by many haematopoietic and non-haematopoietic tissues. It exists as a membrane-associated protein, as well as in an active, soluble form (herein called sDPP4), present at high concentrations in bodily fluids. Despite the proposed use of sDPP4 as a biomarker for multiple diseases, its cellular sources are not well defined. Here, we report that individuals with congenital lymphocyte immunodeficiency had markedly lower serum concentrations of sDPP4, which were restored upon successful treatment and restoration of lymphocyte haematopoiesis. Using irradiated lymphopenic mice and wild-type to Dpp4–/– reciprocal bone marrow chimeric animals, we found that haematopoietic cells were a major source of circulating sDPP4. Furthermore, activation of human and mouse T lymphocytes resulted in increased sDPP4, providing a mechanistic link between immune system activation and sDPP4 concentration. Finally, we observed that acute viral infection induced a transient increase in sDPP4, which correlated with the expansion of antigen-specific CD8+T cell responses. Our study demonstrates that sDPP4 concentrations are determined by the frequency and activation state of lymphocyte populations. Insights from these studies will support the use of sDPP4 concentration as a biomarker for inflammatory and infectious diseases.
2018
nov-2018
Inglese
Blackwell Publishing Ltd
194
2
166
179
14
Pubblicato
Esperti anonimi
Internazionale
Goal 3: Good health and well-being
chemokines
immunodeficiency diseases
T cells
Lymphocytes are a major source of circulating soluble dipeptidyl peptidase 4 / Casrouge, A.; Sauer, A. V.; Barreira Da Silva, R.; Tejera-Alhambra, M.; Sanchez-Ramon, S.; Cancrini, C.; Ingersoll, M. A.; Aiuti, A.; Albert, M. L.. - In: CLINICAL AND EXPERIMENTAL IMMUNOLOGY. - ISSN 0009-9104. - 194:2(2018), pp. 166-179. [10.1111/cei.13163]
none
9
info:eu-repo/semantics/article
262
Casrouge, A.; Sauer, A. V.; Barreira Da Silva, R.; Tejera-Alhambra, M.; Sanchez-Ramon, S.; Cancrini, C.; Ingersoll, M. A.; Aiuti, A.; Albert, M. L....espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/201819
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