AI Article Synopsis

  • HIV infection decreases the transfer of antibodies from mother to fetus, particularly affecting the levels of immunoglobulin G (IgG) specific to malaria and tetanus antigens in newborns.
  • The study measured IgG levels in 107 mother-cord pairs, finding that HIV+ mothers had significantly lower IgG levels for certain antigens, and their neonates had reduced cord IgG.
  • Maternal hypergammaglobulinemia was prevalent among HIV+ women and was linked to lower transplacental antibody transfer, suggesting it may contribute to the reduced antibody levels observed in their infants.

Article Abstract

 Human immunodeficiency virus (HIV) infection reduces placental transfer of antibodies from mother to the fetus for many antigens; however, conflicting data exist for transfer of immunoglobulin G (IgG) to malarial antigens. The mechanism(s) underlying reduced placental transfer is unknown.  Levels of maternal and cord total IgG, IgG subclasses, and cord-to-mother ratios (CMRs) were measured in 107 mother-cord pairs to 3 malarial antigens: circumsporozoite protein (CSP), apical membrane antigen 1 (AMA-1), merozoite surface protein 1 (MSP-1), and tetanus toxoid C-fragment (TTc).  Immunoglobulin G levels to CSP and TTc were lower in HIV+ mothers, and cord IgG to CSP, MSP-1, and TTc were significantly lower in neonates born to HIV+ mothers (all values <.05). The prevalence of mothers with hypergammaglobulinemia was significantly higher among HIV+ women (68%) compared with HIV- mothers (8%) ( < .0001). Maternal hypergammaglobulinemia was associated with reduction in transplacental transfer of antibodies to CSP ( = .03), MSP-1 ( = .004), and TTc ( = .012), and CMRs <1 were found for MSP-1 (odds ratio [OR] = 6.5), TTc (OR = 4.95), and IgG1 to CSP (OR = 3.75, = .025) in statistical models adjusted for maternal IgG.  Data confirmed that HIV infections are associated with lower cord antibody levels to malarial antigens and that hypergammaglobulinemia may contribute to reduced antibody transfer.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4943556PMC
http://dx.doi.org/10.1093/ofid/ofw092DOI Listing

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