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
Affiliations
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.
Immune Checkpoint Inhibition in Hodgkin Lymphoma.
Moy R, Younes A Hemasphere. 2019; 2(1):e20.
PMID: 31723749 PMC: 6745954. DOI: 10.1097/HS9.0000000000000020.
Patel S, Weirather J, Lipschitz M, Lako A, Chen P, Griffin G Blood. 2019; 134(23):2059-2069.
PMID: 31697809 PMC: 7218752. DOI: 10.1182/blood.2019002206.
The immune microenvironment in Hodgkin lymphoma: T cells, B cells, and immune checkpoints.
Vardhana S, Younes A Haematologica. 2016; 101(7):794-802.
PMID: 27365459 PMC: 5004458. DOI: 10.3324/haematol.2015.132761.
Immune suppression in tumors as a surmountable obstacle to clinical efficacy of cancer vaccines.
Wieers G, Demotte N, Godelaine D, van der Bruggen P Cancers (Basel). 2013; 3(3):2904-54.
PMID: 24212939 PMC: 3759179. DOI: 10.3390/cancers3032904.
Arguello R, Albareda M, Alvarez M, Bertocchi G, Armenti A, Vigliano C PLoS One. 2012; 7(5):e35966.
PMID: 22574131 PMC: 3344843. DOI: 10.1371/journal.pone.0035966.