Viral suppression is associated with HIV-antibody level and HIV-1 DNA detectability in early treated children at 2 years of age.
Viral suppression is associated with HIV-antibody level and HIV-1 DNA detectability in early treated children at 2 years of age.
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DOI:
10.1097/qad.0000000000002861
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发表时间:
2021-07-01
期刊:
影响因子:
--
通讯作者:
van Zyl GU
中科院分区:
文献类型:
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作者:
Veldsman KA;Laughton B;Janse van Rensburg A;Zuidewind P;Dobbels E;Barnabas S;Fry S;Cotton MF;van Zyl GU
Early infant HIV diagnosis and antiretroviral therapy (ART) initiation are now implemented shortly after birth. Maintaining and monitoring ART adherence is difficult and requires frequent visits. We therefore investigated whether HIV antibodies and HIV-1 DNA levels are markers of cumulative viremia. We conducted a cross sectional investigation at 2-years-of-age of HIV antibodies and HIV-1 DNA levels in a well-characterized cohort of 31 children who started ART shortly after birth. HIV antibodies were measured by a combination of the Abbott® ARCHITECT® HIV Ag/Ab Combo and Geenius HIV 1/2 supplemental assays; and total HIV-1 DNA quantified using a sensitive qPCR assay targeting the HIV-1 integrase gene. Infant post exposure prophylaxis consisted of zidovudine (AZT) and nevirapine (NPV) (or NVP only, in one child) within 1 day of birth, transitioning, after positive diagnosis, to 3 drug ART, at a median (IQR) of 7 (4-9.5) days. Twelve of 31 children had well-suppressed HIV plasma viral loads (HIVVL) and the remainder periods of viremia (HIVVL > 100 copies/mL after 3 months of ART), classified as non-suppressed. At 24-months-of-age: 11/12 (92%) of well-suppressed children had undetectable HIV-1 antibodies versus 3/19 (16%) non-suppressed children (p<0.001) and 7/12 (58%) well-suppressed children had undetectable HIV-1 DNA versus 3/19 (16%) of non-suppressed children (p=0.02). Considering low assay costs and the high proportion of well-suppressed children with undetected antibody levels at 2 years, HIV antibody levels may be a valuable marker of cumulative adherence in children who start treatment shortly after birth and could prompt adherence and viral load investigation.