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Published on: October 6, 2016
Mannose-binding lectin concentrations in people living with HIV/AIDS infected by HHV-8
Viviane Martha Santos de Morais1, Juliana Prado Gonçales1, Georgea Gertrudes de Oliveira Mendes Cahú1
1Virology Division, Laboratory of Immunopathology Keizo Asami (LIKA), Federal University of Pernambuco, Recife, Pernambuco, Brazil.
Background:
Mannose-binding lectin (MBL) plays an important role in the innate immune response by activating the complement system via the lectin pathway, and it has been studied in several viral infections; however, the influence of MBL in PLWHA infected with HHV-8 is unknown. The objective of this study was to verify the association of MBL deficient plasma concentrations in HIV/HHV-8 coinfected and HIV monoinfected patients and to correlate these concentrations with HIV viral load and CD4 counts in both groups.
Results:
This was an analytical study of case-controls consisting of PLWHA monitored at the medical outpatient of Infectious and Parasitic Diseases of the clinical hospital in the Federal University of Pernambuco. Plasma concentrations of MBL were obtained by an enzyme-linked immunosorbent assay (ELISA) using a commercial Human Mannose Binding Lectin kit (MyBioSource, Inc.) that was performed according to the manufacturer's guidelines, with values < 100 ng/ml considered deficient. A total of 245 PLWHA samples were analysed; 118 were HIV/HHV-8 coinfected and 127 were HIV monoinfected; 5.1% (6/118) of the coinfected patients and 3.2% (4/127) of the monoinfected patients (p = 0.445) were considered plasma concentration deficient. The median of the plasma concentrations of MBL in the coinfected patients was 2803 log10 ng/ml and was 2.959 log10 ng/ml in the monoinfected patients (p = 0.001). There was an inverse correlation between the plasma concentrations of MBL and the HIV viral load in both groups, but no correlation with the CD4 count.
Conclusions:
Although the plasma concentrations considered deficient in MBL were not associated with HHV-8 infection in PLWHA, the coinfected patients showed lower MBL concentrations and an inverse correlation with HIV viral load, suggesting that there may be consumption and reduction of MBL due to opsonization of HIV and HHV-8, leading to the reduction of plasma MBL and non-accumulation in the circulation.
Insights
Mannose-binding lectin (MBL) levels were lower in HIV/HHV-8 coinfected individuals compared to HIV-only patients. Lower MBL concentrations correlated with higher HIV viral load, suggesting MBL consumption during coinfection.
Area of Science:
- Immunology
- Virology
- Infectious Diseases
Background:
- Mannose-binding lectin (MBL) is crucial for innate immunity, activating the complement system via the lectin pathway.
- MBL's role in viral infections is established, but its influence in individuals with Human Immunodeficiency Virus (HIV) and Human Herpesvirus 8 (HHV-8) coinfection was previously unknown.
Purpose of the Study:
- To investigate the association of MBL-deficient plasma concentrations in HIV-infected individuals with or without HHV-8 coinfection.
- To correlate MBL plasma concentrations with HIV viral load and CD4+ T-cell counts in both patient groups.
Main Methods:
- An analytical case-control study involving 245 people living with HIV/AIDS (PLWHA).
- Plasma MBL concentrations were measured using ELISA, with values < 100 ng/ml defined as deficient.
- Samples included 118 HIV/HHV-8 coinfected and 127 HIV monoinfected patients.
Main Results:
- MBL-deficient plasma concentrations were found in 5.1% of coinfected and 3.2% of monoinfected patients (p=0.445).
- Median MBL plasma concentrations were significantly lower in coinfected patients (2803 log10 ng/ml) compared to monoinfected patients (2959 log10 ng/ml) (p=0.001).
- An inverse correlation was observed between MBL plasma concentrations and HIV viral load in both groups; no correlation with CD4 count was found.
Conclusions:
- MBL deficiency was not significantly associated with HHV-8 coinfection in PLWHA.
- HIV/HHV-8 coinfected patients exhibited lower MBL concentrations, inversely correlated with HIV viral load.
- This suggests potential MBL consumption and reduction due to opsonization of HIV and HHV-8, leading to decreased circulating MBL levels.
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