To investigate the association of human immunodeficiency virus (HIV) with various DNA viruses, including hepatitis B virus (HBV), cytomegalovirus (CMV) and Epstein-Barr virus, (EBV), simultaneous detection of HIV p24 antigen, HBV surface antigen and DNA, CMV-DNA and EBV-DNA expression was performed in phytohemagglutinin-stimulated peripheral blood mononuclear (PBMC) culture supernatants obtained from 54 individuals at risk for HIV infection. HIV expression in PBMC culture supernatants never occurred alone; expression of other viruses was always detected in the 24 samples expressing HIV antigen in vitro. Furthermore, in 16 patients expression of other viruses was detected without HIV expression, and in 14 patients none of the tested viruses were detected. These results indicate a strong association between the presence of HIV antibody and expression of DNA viruses in vitro (p = 0.0001). The coexpression of these viruses could be related to the evolution of HIV infection and AIDS.

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HIV-1 seronegative patients at high risk for HIV infection were followed up. In 1990 PCR was positive for HIV DNA sequences in samples of 17 seronegative patients who continued to report for surveillance of HIV infection. There was clear evidence of seroconversion in four of these 17 seronegative patients, while in one patient an indeterminate result for HIV was repeatedly obtained in different samples. The other 12 patients continue to be seronegative without any evidence of HIV infection except the presence of provirus in peripheral blood mononuclear cells. It is important to apply the PCR technique together with tests to detect other virological and immunological markers, in order to identify seronegative carriers and thus avoid HIV transmission by them.

The polymerase chain reaction (PCR) was used to analyze the presence of hepatitis B virus (HBV) DNA in serum and peripheral blood mononuclear cells (PBMCs) from 20 patients with AIDS with and without conventional HBV serological markers. DNA sequences of HBV were detected in PBMCs from 13 patients, nine of whom were positive for anti-HBc only and four of whom were also positive for anti-HBs. When PBMCs from patients were activated in culture with phytohemagglutinin, the presence of HBsAg could be detected in the culture supernatants from four of 13 patients with HBV DNA in their PBMCs; for two of the four, HBV DNA could also be detected in the culture supernatant after DNA amplification. It was observed that HBV DNA sequences found in PBMCs can be reactivated by mitogen stimulation in some HIV-1 infected patients.

The complement system is one of the host’s primary defence mechanisms against pathogens. Its activation involves proteolytic cascades of enzymatic reactions that result in products with effector functions and recognition of molecules on the surface of microorganisms [1,2].