Abstract

Background

HLA-G, a non-classical HLA class I antigen, is of crucial interest during pregnancy by inhibiting maternal immune response. Its role during infections is discussed, and it has been described that high levels of soluble HLA-G during childhood increase the risk of malaria. To explore more precisely interactions between soluble HLA-G and malaria, latent class analysis was used to test whether distinct sub-populations of children, each with distinctive soluble HLA-G evolutions may suggest the existence of groups presenting variable malaria susceptibility.

Method

A study was conducted in Benin from 2010 to 2013 and 165 children were followed from birth to 12 months. Evolution of soluble HLA-G was studied by the latent class method.

Results

Three groups of children were identified: one with consistently low levels of soluble HLA-G during follow-up, a second with very high levels and a last intermediate group. In all groups, low birth weight, high number of malaria infections and high exposure to malaria transmission were associated with high level of soluble HLA-G. Placental malaria was not. Presence of soluble HLA-G in cord blood increased the probability of belonging to the highest trajectory.

Conclusion

These results, together with previous ones, confirm the important role of HLA-G in the individual susceptibility to malaria. Assaying soluble HLA-G at birth could be a good indicator of newborns more fragile and at risk of infections during childhood.

Details

Title
Evolution of the levels of human leukocyte antigen G (HLA-G) in Beninese infant during the first year of life in a malaria endemic area: using latent class analysis
Author
dAlmeida, Tania C; Ibrahim Sadissou; Cottrell, Gilles; Tahar, Rachida; Moreau, Philippe; Favier, Benoit; Moutairou, Kabirou; Donadi, Eduardo A; Massougbodji, Achille; Rouass-Freiss, Nathalie; Courtin, David; Garcia, Andre
Pages
n/a
Publication year
2016
Publication date
2016
Publisher
Springer Nature B.V.
e-ISSN
14752875
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
1798361573
Copyright
Copyright BioMed Central 2016