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Human CTLA-4 is Expressed in Situ on T Lymphocytes in Germinal Centers, in Cutaneous Graft-versus-host Disease, and in Hodgkin's Disease

Overview
Journal Am J Pathol
Publisher Elsevier
Specialty Pathology
Date 1998 Apr 18
PMID 9546357
Citations 8
Authors
Affiliations
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Abstract

Cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4, CD152) is a molecule expressed on in vitro activated T cells. CTLA-4 shares important sequence homology with CD28 and binds to the same ligands, CD80 (B7-1) and CD86 (B7-2). CTLA-4 probably functions as a negative regulator of T lymphocyte activation in the mouse, although this remains to be proven for human T lymphocytes. We have developed new monoclonal antibodies against human CTLA-4 and have investigated the in situ expression of CTLA-4 in a wide variety of normal and pathological human tissues expressing CD80 and CD86. As revealed in this study, CTLA-4 is expressed on thymocytes in thymic medulla, on a subset of CD4+ T lymphocytes in germinal centers of follicular hyperplasia, on T cells, mainly CD8+, infiltrating skin affected by graft-versus-host disease, and on T cells, mainly CD4+, infiltrating Hodgkin's disease lesions. In immunoelectron microscopy, CTLA-4 was found on the plasma membrane as well as in the hyaloplasm and cytoplasmic vesicles, in agreement with its pattern of expression on in vitro activated T cells. Interestingly, no or at most scarce expression of CTLA-4 was found in granulomatous lymph nodes, T-cell-mediated inflammatory diseases, or non-Hodgkin's lymphomas, regardless of their expression of CD80 or CD86. Thus, expression of CTLA-4 appears to be induced in selective pathological conditions in vivo. The pathways leading to selective induction of CTLA-4 and its role in the pathophysiology of these conditions need to be further investigated.

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References
1.
Wagner Jr D, Hagman J, Linsley P, Hodsdon W, Freed J, Newell M . Rescue of thymocytes from glucocorticoid-induced cell death mediated by CD28/CTLA-4 costimulatory interactions with B7-1/B7-2. J Exp Med. 1996; 184(5):1631-8. PMC: 2192898. DOI: 10.1084/jem.184.5.1631. View

2.
Leung H, Bradshaw J, Cleaveland J, Linsley P . Cytotoxic T lymphocyte-associated molecule-4, a high-avidity receptor for CD80 and CD86, contains an intracellular localization motif in its cytoplasmic tail. J Biol Chem. 1995; 270(42):25107-14. DOI: 10.1074/jbc.270.42.25107. View

3.
Bluestone J . Is CTLA-4 a master switch for peripheral T cell tolerance?. J Immunol. 1997; 158(5):1989-93. View

4.
Castan J, Tenner-Racz K, Racz P, Fleischer B, Broker B . Accumulation of CTLA-4 expressing T lymphocytes in the germinal centres of human lymphoid tissues. Immunology. 1997; 90(2):265-71. PMC: 1456743. DOI: 10.1046/j.1365-2567.1997.00162.x. View

5.
Kosco-Vilbois M, Zentgraf H, Gerdes J, Bonnefoy J . To 'B' or not to 'B' a germinal center?. Immunol Today. 1997; 18(5):225-30. DOI: 10.1016/s0167-5699(97)01048-7. View