CIRCULATING IMMUNE-COMPLEXES IN HUMAN TUBERCULOSIS SERA - DEMONSTRATION OF SPECIFIC ANTIBODIES AGAINST MYCOBACTERIUM-TUBERCULOSIS GLYCOLIPID (DAT, PGLTB1, LOS) ANTIGENS IN ISOLATED CIRCULATING IMMUNE-COMPLEXES
N. Simonney et al., CIRCULATING IMMUNE-COMPLEXES IN HUMAN TUBERCULOSIS SERA - DEMONSTRATION OF SPECIFIC ANTIBODIES AGAINST MYCOBACTERIUM-TUBERCULOSIS GLYCOLIPID (DAT, PGLTB1, LOS) ANTIGENS IN ISOLATED CIRCULATING IMMUNE-COMPLEXES, European journal of clinical investigation, 27(2), 1997, pp. 128-134
Citations number
22
Categorie Soggetti
Medicine, Research & Experimental","Medicine, General & Internal
An enzyme-linked immunosorbent assay (ELISA) for IgG using three glyco
lipid antigens from Mycobacterium tuberculosis in 65 tuberculosis (TB)
patients and 50 healthy control subjects was performed. The circulati
ng immune complexes (CICs) were isolated by precipitation with polyeth
ylene glycol 6000 (PEG). This method associated to ELISA measured the
specific antibodies present in these CICs. PEG [optical density (OD) 2
80] was shown to be significantly elevated (P <.0.001) in tuberculous
samples. The concentrations of IgG antibodies complexed to the three g
lycolipid antigens were shown to be higher in patient with tuberculosi
s than in normal control subjects (P <0.001). No correlation was obser
ved between levels of free and CIC-bound antibodies. These antibodies
isolated from CICs were responsible for almost all of the false-negati
ve serological results. However, great heterogeneity was noticed depen
ding on the antigen used, showing a more positive ELISAs against DAT (
77%) than against LOS (71%) or PGLTb1 (18.5%). No correlation was esta
blished between the presence of specific CIC-complexed IgG and the bac
teriological load or the tuberculosis localization (pulmonary vs. extr
apulmonary). The sensitivity of ELISA for CIC-complexed IgG to DAT and
LOS was lower in HIV-infected TB patients. From these results, we con
clude that detection of complexed IgG DAT and LOS glycolipid antigen w
ill be useful as a complementary technique for the serodiagnosis of tu
berculosis.