MAPPING OF 2 NEW HUMAN B-CELL EPITOPES ON HIV-1 GP120

Objective: To map epitopes on gp120 defined by human antibodies and to examine the neutralizing activity of these antibodies. Design and methods: Serum from HIV-1-antibody-positive individuals was used to screen a random fragment expression library representing gp120 from the HIV(IIIB) clone BH10. The library was based on the pUEX1 expression vector. Serum was tested for in vitro neutralizing activity using H9 cells and the HIV(IIIB) isolate. Results: Four different epitopes defined by human antibodies were mapped on gp120. Two of these have not previously been reported and are located within amino acids (aa) 90-100 in the C1 region and aa 355-365 in the semi-conserved region between V3 and V4. The other two are located within aa 140-145 and aa 286-309. These epitopes are situated in regions that have been shown to demarcate human epitopes. Three serum samples with neutralization titres greater-than-or-equal-to 1024 were identified. None of the purified antibody fractions defining the mapped epitopes on gp120 had any neutralizing capacity against HIV(IIIB). Conclusions: This study is the first demonstration of the applicability of random fragment expression libraries for the direct screening of human serum in order to map epitopes on gp120. Two new epitopes and two previously identified epitopes were mapped in this way. However, none of the linear epitopes was defined by antibody fractions neutralizing HIV(IIIB), and it was not possible to map epitopes defined by neutralizing antibodies in the serum samples capable of neutralizing HIV(IIIB) infection of H9 cells. Thus, it appears that the neutralizing activity of serum in this study was not due to anti-gp120 antibodies defining linear epitopes.