The sera of 33 HIV-1-infected individuals, previously shown to neutral
ize HIV-1(MN) in vitro, were screened by ELISA for IgA reactivity agai
nst rgpl20(MN) and a synthetic V3(MN) loop peptide. Six were selected
for evaluation of the effect of serum IgA from infected individuals on
the in vitro infection of susceptible target cells by HIV-1(MN). By u
sing protein C immobilized on Sepharose, we depleted the sera of Ige t
o a level undetectable by nephelometry and viral envelope-specific ELI
SA. The IgA component of the IgG-depleted serum was affinity purified
with immobilized jacalin, a lectin that selectively binds the IgA1 fra
ction of human Ig. Igc-depleted sera and purified IgA1 serum fractions
showing IgA reactivity against rgp120(MN) and V3(MN) by ELISA inhibit
ed the in vitro infection of CEM-ss cells by HIV-1(MN), but sera deple
ted of both IgG and IgA1 did not. These data show that, like serum IgG
, serum IgA from selected HIV-1-infected individuals is capable of neu
tralizing HIV-1(MN) in vitro. The biologic significance of this observ
ation and the identities of serum IgA-recognized HIV-1 neutralization
epitopes remain to be determined.