In human cultured monocytic cells stimulated by cytokines, CD43 was demonst
rated to exhibit a modification of sialylated epitopes (dys-sialylation) [S
oler et al: Leukoc Bio[ 1997;61:609-618]. Therefore, we chose to investigat
e CD43 behavior on patients who present pathological status implicating mon
ocytes after renal graft (KTR). We performed flow cytometry after immune st
aining using monoclonal antibodies to CD43 sialic acid-dependent (L60) and
-independent (L10) epitopes, Compared to normal controls, mean fluorescence
intensity was never altered on lymphocytes. Conversely, on monocytes, we f
ound different profiles with L60: 26% of patients having normal CD43 expres
sion, 54% displayed decreased values and 20% had a double population of mon
ocytes, the major one being normal and the minor one with a very low staini
ng, Decreased values were more frequent among KTR during the first 3 months
following transplantation. L10 immunostaining was not altered on monocytes
in patients with low values of CD43 staining by L60, confirming that the m
echanism involved was a CD43 dys-sialylation. We investigated a possible ro
le of cyclosporin (CsA) on human monocytic (THP-1) and lymphoid (Jurkat) ce
ll lines. CsA decreases CD43 expression in monocytic and not in lymphoid ce
ll lines and could be responsible for the specific dys-sialylation of KTR m
onocytes. Whatever, CD43 dys-sialylation might lead to functional abnormali
ties of monocytes in KTR, possibly involving the adhesion process. Copyrigh
t (C) 2000 S. Karger AG, Basel.