SUBPOPULATIONS OF T-LYMPHOCYTES IN THE PERIPHERAL-BLOOD, DERMAL LESIONS AND LYMPH-NODES OF POST KALA-AZAR DERMAL LEISHMANIASIS PATIENTS

Citation
Mk. Ghosh et al., SUBPOPULATIONS OF T-LYMPHOCYTES IN THE PERIPHERAL-BLOOD, DERMAL LESIONS AND LYMPH-NODES OF POST KALA-AZAR DERMAL LEISHMANIASIS PATIENTS, Scandinavian journal of immunology, 41(1), 1995, pp. 11-17
Citations number
34
Categorie Soggetti
Immunology
ISSN journal
03009475
Volume
41
Issue
1
Year of publication
1995
Pages
11 - 17
Database
ISI
SICI code
0300-9475(1995)41:1<11:SOTITP>2.0.ZU;2-5
Abstract
Distribution of different subpopulations of T cells in the dermal lesi ons, lymph nodes and peripheral blood of post kala-azar dermal leishma niasis (PKADL) patients was studied by using appropriate phenotypic ma rkers for CD2(+), CD4(+) and CD8(+) cells. Histopathological studies o f skin lesions showed marginal to massive infiltration of mononuclear cells depending upon the duration of illness and type of lesions. Thus , while the hypopigmented patches were represented by small focal coll ections of lymphocytes with scanty parasites in the dermis, these were replaced at the nodular stage with massive granulomas consisting of l ymphocytes, plasma cells and histiocytes with numerous amastigotes. Th e involvement of CD4(+) and CD8(+) cell types in these lesions also sh owed a gradual change from the appearance of a few cells of both the p henotypes in early hypopigmented type to massive accumulation of cells , primarily of CD8(+) phenotype, in the granuloma of nodular type. How ever, the observed preponderance of CD8(+) cells at the lesion site of chronic PKADL patients is in contrast to their peripheral blood CD4()/CD8(+) cell ratio (1.9:1) which remained within the normal limits. S imilar studies of lymph nodes from PKADL patients with lymphadenopathy revealed infiltration of the cortical areas by T cells which were mor e of CD8(+) than CD4(+) phenotypes. All these results document the inv olvement of CD8(+) cells in leishmanoid lesions. Thus, it is likely th at these cells, in association with appropriate subpopulations of CD4( +) cells, play a profound role in the evolution of dermal pathology in PKADL.