Quality of T-Cell Response to SARS-CoV-2 mRNA Vaccine in ART-Treated PLWH.
Eeva TortelliniMaria Antonella ZingaropoliGiulia MancarellaRaffaella MaroccoAnna CarraroMeriem JamhourChristian BarbatoMariasilvia GuardianiFederica DominelliPatrizia PasculliAnna NapoliAurelia GaetaFabio MengoniPaola ZuccalàValeria BelvisiBlerta KertushaAlberico ParenteCosmo Del BorgoVincenzo VulloMaria Rosa CiardiClaudio Maria MastroianniMiriam Lichtnernull Latina Covid-GroupPublished in: International journal of molecular sciences (2022)
We investigated specific humoral and T-cell responses in people living with HIV (PLWH) before (T0), after two (T1) and after six months (T2) from the third dose of the BNT162b2 vaccine. Healthy donors (HD) were enrolled. The specific humoral response was present in most PLWH already after the second dose, but the third dose increased both the rate of response and its magnitude. Collectively, no significant differences were found in the percentage of responding T-cells between PLWH and HD. At T0, stratifying PLWH according to CD4 cell count, a lower percentage of responding T-cells in <200 cells/µL subgroup compared to >200 cells/µL one was observed. At T1, this parameter was comparable between the two subgroups, and the same result was found at T2. However, the pattern of co-expression of IFNγ, IL2 and TNFα in PLWH was characterized by a higher expression of TNFα, independently of CD4 cell count, indicating a persistent immunological signature despite successful ART. mRNA vaccination elicited a specific response in most PLWH, although the cellular one seems qualitatively inferior compared to HD. Therefore, an understanding of the T-cell quality dynamic is needed to determine the best vaccination strategy and, in general, the capability of immune response in ART-treated PLWH.
Keyphrases
- immune response
- sars cov
- induced apoptosis
- poor prognosis
- rheumatoid arthritis
- binding protein
- single cell
- cell cycle arrest
- hiv infected
- randomized controlled trial
- dendritic cells
- clinical trial
- antiretroviral therapy
- stem cells
- quality improvement
- endoplasmic reticulum stress
- mass spectrometry
- cell death
- nk cells
- study protocol
- high resolution