W. Zhuge et al., FAILURE OF SIVMAC TO BE NEUTRALIZED IN MACROPHAGE CULTURES IS UNIQUE TO SIVMAC AND NOT OBSERVED WITH NEUTRALIZATION OF SHIV OR HIV-1, AIDS research and human retroviruses, 14(12), 1998, pp. 1045-1051
Except during acutely lethal infection, macaques infected with SIV(mac
)251 produce antibodies that neutralize the virus in CEMx174 cells, ma
caque PBMC and macrophage cultures. In a previous report, we had shown
that whereas neutralization of the SIV(mac)251 was complete in lympho
cyte cultures, ''protected'' macrophages had actually become latently
infected, and remained viral DNA-positive, but the infection was nonpr
oductive as long as antibodies were maintained in the medium. Removal
of the antibodies as long as 1 week later, resulted in resurgence of v
irus replication. In the present study, we compared neutralization of
SIV(mac)239 with that of neutralization of SHIV and HIV-1, and sought
to determine whether the failure to prevent infection in macrophages w
as also typical of neutralization of SHIV and HIV-1 in macaque and hum
an macrophage cultures, respectively. The results showed that similar
to SIV(mac)251, neutralizing antibodies did not block SIV(mac)239 infe
ction in macaque macrophages, although they blocked infection of the v
irus in T cells. The data from neutralization of SHIV using anti-SHIV
antibodies and for neutralization of HIV-1 (89.6 and Bal) using anti-H
IV IgG in both T cells and macrophages, however, can be summarized wit
h a single statement: neutralization of SHIV and HIV-1 was complete in
all of the cultures, with no evidence of establishment of latent infe
ction in or resurgence of virus replication after antibodies were remo
ved from macrophage cultures. The non-neutralizability of SIVmac (251
and 239) in macrophages is therefore unique to the SIVmac and not rele
vant to neutralization of HIV-1.