Lymphocytes are a major source of circulating soluble dipeptidyl peptidase 4

Author:

Casrouge A12,Sauer A V3,Barreira da Silva R4,Tejera-Alhambra M5,Sánchez-Ramón S5,Cancrini C67,Ingersoll M A12,Aiuti A3,Albert M L124,

Affiliation:

1. Laboratory of Dendritic Cell Biology, Department of Immunology, Institut Pasteur, Paris, France

2. INSERM U1223, Paris, France

3. San Raffaele Telethon Institute for Gene Therapy (SR-TIGET), San Raffaele Scientific Institute, Milan, Italy

4. Department of Cancer Immunology, Genentech, Inc, South San Francisco, CA, USA

5. Servicio de Inmunología. Hospital Clínico San Carlos, Madrid, Hospital General Universitario Gregorio Marañón, Madrid, Spain

6. Ospedale Pediatrico, Bambino Gesù, Roma, Italy

7. University Department of Pediatrics, Unit of Immune and Infectious Diseases, Childrens' Hospital Bambino Gesù-University of Torvergata Rome, Rome, Italy

Abstract

Summary 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.

Funder

National Institutes of Health grant

Starzl Transplantation Institute

Institut Pasteur

Ligue Contre le Cancer

Fondation ARC

Ministero della Salute

European Union Seventh Framework Programme

Agence Nationale de la Recherche

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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