CD4(+) T cells are critical for corneal, but not skin, allograft rejection

Citation
Z. Haskova et al., CD4(+) T cells are critical for corneal, but not skin, allograft rejection, TRANSPLANT, 69(4), 2000, pp. 483-487
Citations number
27
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
TRANSPLANTATION
ISSN journal
00411337 → ACNP
Volume
69
Issue
4
Year of publication
2000
Pages
483 - 487
Database
ISI
SICI code
0041-1337(20000227)69:4<483:CTCACF>2.0.ZU;2-4
Abstract
Background. The relative contribution of CD4(+) or CD8(+) T cells in allogr aft rejection remains to be fully characterized. Some reports indicate that there is an absolute requirement for CD4(+) T cells in allogeneic rejectio n, whereas others report that CD4-depleted mice are capable of rejecting ce rtain types of allografts. Methods. We compared the ability of CD4(-) knockout (KO), CD8(-) KO, and no rmal CD4(+)/CD8(+) mice to reject allogeneic corneal or skin grafts. We als o examined delayed-type hypersensitivity and CTL responses to donor alloant igens, Results. Engraftment of C57BL/6 corneas to C.B6-(n5-7) CD4(-)KO mice result ed in significantly higher rates of acceptance (>85%) than either C.B6-(n5- 7) CD8(-) KO (30%) or normal BALB/c mice (40%). Likewise, mean survival tim es for B6 skin grafts placed on C.B6-(n5-7) CD4(-) KO mice (29.2 +/- 3.5 da ys) were significantly increased over those of normal BALB/c mice (13.2 +/- 1 days), although most CD4(-) KO mice (70%) eventually reject their grafts . C.B6-(n5-7) CD4(-) KO mice that reject allogeneic grafts fail to develop a delayed-type hypersensitivity response, but they did demonstrate signific antly greater cytotoxic T lymphocyte precursor (CTLp) frequencies than did CD4(-) KO mice that accepted such grafts or that were not grafted. Conclusions. This study indicates that mice lacking CD4(+) T cells have a s ignificantly impaired ability to reject corneal allografts, but are able, i n most cases, to reject allogeneic skin grafts. Thus, in the absence of CD4 (+) T cells, the likely mechanism for rejection appears to involve the gene ration of CD8(+) CTLs.