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Persons at risk for
HIV-2 infection include:
Sex partners of a
person from a country where HIV-2 is endemic (this category includes
persons originally from such countries).
Sex partners of a
person known to be infected with HIV-2.
Persons who
received a transfusion of blood or a nonsterile injection in a country
where HIV-2 is endemic.
Persons who shared
needles with a person from a country where HIV-2 is endemic or with a
person known to be infected with HIV-2.
Children of women
who have risk factors for HIV-2 infection or who are known to be
infected with HIV-2.
Additionally,
testing for HIV-2 is indicated when there is clinical evidence for or
suspicion of HIV disease (such as an AIDS-associated opportunistic
infection) in the absence of a positive test for antibodies to HIV-1 and
in cases in which the HIV-1 Western blot exhibits the unusual
indeterminate pattern of gag (p55, p24, or p17) plus pol (p66, p51, or
p32) bands in the absence of env (gp160, gp120, Or gp41) bands.
Although most HIV
infections in the United States are of HIV-1 group B subtype, current
ELISAs can accurately identify infections with nearly all non-B subtypes
and many infections with group O HIV subtypes. Infections with HIV-2 and
HIV-1 group O are rare in the United States and routine screening for
these subtypes is not generally recommended as part of diagnostic
testing except in areas where several such infections have been
identified. Routine screening for HIV-2 might be appropriate in certain
populations where potential risk for HIV-2 infection is higher (e.g., in
areas where West African immigrants have settled). Since June 1992, FDA
has recommended routine screening for antibody to HIV-2 (in addition to
HIV-1) for all blood and plasma donations. Clients with clinical,
epidemiologic, or laboratory history that suggests HIV infection and
negative or indeterminate HIV-1 screening tests should receive further
diagnostic testing to rule out HIV infection, potentially including
testing for HIV-1 non-B subtypes and HIV-2 .
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