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Cervicovaginal synthesis of IgG antibodies to the immunodominant 175–199 domain of the surface glycoprotein gp46 of human T-cell leukemia virus type I

✍ Scribed by Bélec, Laurent; Georges-Courbot, Marie-Claude; Georges, Alain; Mohamed, Ali Si; Londos-Gagliardi, Danielle; Hallouin, Marie-Charlotte; Hocini, Hakim; Guillemain, Bernard


Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
898 KB
Volume
50
Category
Article
ISSN
0146-6615

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✦ Synopsis


Paired sera, saliva and cervicovaginal secretions from 17 HTLV-I-infected women (19-75 yr) were tested for total IgA and IgG, for IgA and IgG to the immunodominant region gp46/175-Pro-199, for serum IgG to the neutralizing domains gp46/ 190-Pro-I99 and gp46/190-Ser-199, or for tax-rex proviral HTLV-DNA. Serum antibodies to gp46/ 175-Pro-I99 were detected more frequently in the IgG (13/17) than in the IgA (5/17) isotypes. The majority (8/12) of anti-gp46/175-Pro-199-positive sera reacted also to gp46/190-Pro-199 or to gp46/ 190-Ser-199, demonstrating their neutralizing properties. In saliva, antibodies to gp46/175-Pro-199were notgenerallydetected. In cervicovaginal secretions, IgG to gp46/175-Pro-199, but not IgA, were detected in 6/15 (40%) patients. The mean specific activity of IgG to gp46/175-Pro-199 showed a trend to be higher in cervicovaginal secretions (218 c 109) than in sera (14 + 4). Furthermore, in all patients with cervicovaginal IgG to g p46/175-Pro-199, the cervicovaginal/seru m ratio (19 2 6) of anti-gp46 IgG specific activities were markedly above 1. HTLV-DNA was detected in 4/17 salivas, and in 3/15 cervicovaginal secretions, all from patients demonstrating cervicovaginal synthesis of IgG to gp46/175-Pro-199. In conclusion, IgG to gp46/175-Pro-199 in cervicovaginal secretions, when present, appear to be produced primarily locally because of local HTLV-I excretion. Since anti-gp46/175-Pro-199 antibodies usually support reactivities to neutralizing domains, their presence could be relevant for limiting HTLV-I transmission via cervicovaginal secretions.


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In order to study the antigenicity of envelope 46 kDa glycoprotein (gp46) of human T-cell leukemia virus type-I (HTLV-I), we have generated monoclonal anti-gp46 antibodies (MAbs), REY-7, REY-I I, REY-16, REY-30, MET4 and MET-3 from rats and mice. lmmunoblot and immunofluorexence assays showed that t