Plasma viral load in HIV-1 and HIV-2 singly and dually infected individuals in Guinea-Bissau, West Africa - Significantly, lower plasma virus set point in HIV-2 infection than in HIV-1 infection
S. Andersson et al., Plasma viral load in HIV-1 and HIV-2 singly and dually infected individuals in Guinea-Bissau, West Africa - Significantly, lower plasma virus set point in HIV-2 infection than in HIV-1 infection, ARCH IN MED, 160(21), 2000, pp. 3286-3293
Citations number
46
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
Background: The intriguing differences in the natural course, transmissibil
ity, and epidemiological characteristics of human immunodeficiency virus ty
pe 1 (HIV-1) and HIV-2 are still insufficiently explained. Differences in p
lasma viral load are an obvious possibility, but this has been difficult to
investigate because of the lack of tests for HIV-2 RNA.
Objective: To compare plasma HIV RNA load between individuals infected with
HIV-1 and HIV-2 in Guinea-Bissau, a West African country with high prevale
nce and incidence of HIV-1 and HIV-2 infection.
Methods A total of 102 participants were recruited from ongoing prospective
cohort studies. These included 19 HIV-1 and 29 HIV-2 seroincident cases te
sted at a median of less than 2 years after seroconversion as well as serop
revalent cases with single (9 HIV-1 cases and 31 HIV-2 cases) or dual (n=14
) infections. Plasma HIV RNA levels were determined by a commercial HIV-1 a
ssay and an experimental HIV-2 assay based on the same principles.
Results: The viral set point, ie, the semi-equilibrium reached after seronc
onversion, was 28-fold lower in recent HIV-2 seroconverters than in recent
HIV-1 seroconverters (median, 2500 and 70 000 RNA copies per milliliter, re
spectively; P<.001). This difference appeared to persist to symptomatic sta
ges of the diseases. Dually infected individuals had lower plasma HIV-I RNA
levels than singly infected individuals.
Conclusions: The differences between HIV-1 and HIV-2 infection are likely t
o be caused by differences in plasma viral set point and load, but the mech
anisms through which HIV-2 infection is contained to a higher degree than H
IV-1 remain to be identified.