Abstract:
Data on baseline characteristics among HIV infected patients is very important especially
among elderly patients seeking critical care. However, this information is widely not
considered in Kenya with those seeking treatment at Kisii Teaching and Referral Hospital
(KTRH) not exceptional. In addition, it is also not clear if HIV intrinsically accelerating
immunosenescence among the elderly HIV-infected persons (EHIP). Despite HIV
prevalence being high among elderly globally, the impact of their baseline characteristics
on HIV infection and immunosenescence acceleration has not yet been evaluated among
elderly HIV infected populations of Kisii. Therefore, this study evaluated the baseline
characteristics and alterations in immunosenescence lymphocyte markers frequencies over
time among the EHIP aged 50 years against elderly HIV uninfected persons (EHUP)
controls. In addition, the relationship between duration of ART and immunosenescence was
also determined. A laboratory-based descriptive, cross-sectional study was performed using
EHIP attending HIV/AIDS clinic at KTRH. Archived data on baseline characteristics of
1329 EHIP, collected retrospectively between January 2008 and December 2019 was used
in this day. A total of 62 HIV infected individuals were sampled from 1329 eligible elderly
HIV infected individuals and their blood samples analysed for T, B and NK cell subsets
and the expression of immunosenescence markers (CD4+ CCR7+
, CD8+CCR7+
, IgD CD27-
and CD56-CD16+
) frequencies using flow cytometry. In addition, theCD4/CD8 ratio
was also determined. Descriptive statistics for summarise for baseline characteristics were
done and compared using the Kruskal-Wallis. Wilcoxon signed-rank test was done in
collating first and last VL based on demographics. Mean divergences for cell count and
proportions of lymphocyte subsets were computed using Student‘s t-test for parametric
values. Linear regression analysis was used in assessing the relationship between age in
years vs. the proportion of cells. The p-values ≤0.05 were considered statistically important.
The results showed that, at the point of recruitment to care, age, WHO AIDS staging,
gender and residence have significant impact on the decline of VL and CD4 count in
elderly persons living with HIV. Substantial deviations on CD3+
, CD4+
, CD8+
,
CD8+CCR7-
and CD4+CCR7-
cells exists between EHIP and the controls (EHUP) with age,
HIV infection and CD4/CD8 ratio being factors attributing to this effect. In addition, there
were substantial differences in cell count and percentages of CD19+
, IgD+CD27+
,
IgD+CD27-
, IgD-CD27-
, and IgD-CD27+
lymphocyte subsets between EHIP and controls
(EHUP). There were also substantial differences in the frequencies of CD56+CD16+
, CD56-
CD16+
, CD56++CD16+
and CD56++CD16- NK cells between EHIP and EHUP. However,
there was no significant relationship between the distribution of T, B, and NK leukocyte
subsets and the duration on ART. This study shows that HIV infection accelerates
immunosenescence in elderly HIV infected people with the baseline characteristics being
predictive of care outcome among EHIP seeking care. This study recommends regular
monitoring and evaluation of baseline characteristics of EHIP as a guide in patients care. In
addition, regular evaluation of; T cell, B cell and NK cell immunosenescence could be a
pathway to promotion of health for the elderly living with HIV.