The prognosis for delayed immune recovery in HIV-infected children might be associated with pre-cART CD4+ T cell count irrespective of co-infection with tuberculosis

Abstract Background Immune reconstitution following the initiation of combination antiretroviral therapy (cART) significantly impacts the prognosis of individuals infected with human immunodeficiency virus (HIV). Our previous studies have indicated that the baseline CD4+ T cells count and percentage...

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Main Authors: Funsho J. Ogunshola, Ruhul A. Khan, Musie Ghebremichael
Format: Article
Language:English
Published: BMC 2025-01-01
Series:BMC Research Notes
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Online Access:https://doi.org/10.1186/s13104-024-07032-y
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author Funsho J. Ogunshola
Ruhul A. Khan
Musie Ghebremichael
author_facet Funsho J. Ogunshola
Ruhul A. Khan
Musie Ghebremichael
author_sort Funsho J. Ogunshola
collection DOAJ
description Abstract Background Immune reconstitution following the initiation of combination antiretroviral therapy (cART) significantly impacts the prognosis of individuals infected with human immunodeficiency virus (HIV). Our previous studies have indicated that the baseline CD4+ T cells count and percentage before cART initiation are predictors of immune recovery in TB-negative children infected with HIV, with TB co-infection potentially causing a delay in immune recovery. However, it remains unclear whether these predictors consistently impact immune reconstitution during long-term intensive cART treatment in TB-negative/positive children infected with HIV. Results We confirmed that the baseline CD4+ T cell count is a significant predictor of immune recovery following long-term intensive cART treatment among children aged 0 to 13 years. Children with lower CD4+ T cell count prior cART initiation did not show substantial immunological recovery during the follow-up period. Interestingly, children who were co-infected with TB and had higher baseline CD4+ T cell count eventually achieved good immunological recovery comparable to the TB-negative HIV-infected children. Hence, the baseline CD4+ T cell count at the onset of treatment serves as a reliable predictor of immunological reconstitution in HIV-infected children with or without TB co-infection. Taken together, this follow-up study validates our previous findings and further establishes that initiating cART early alongside early HIV testing can help prevent the diminished CD4+ T cell count associated with inadequate immunological reconstitution.
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spelling doaj-art-095fc1b568524b9c9a3254360f7db9fe2025-01-12T12:06:50ZengBMCBMC Research Notes1756-05002025-01-011811810.1186/s13104-024-07032-yThe prognosis for delayed immune recovery in HIV-infected children might be associated with pre-cART CD4+ T cell count irrespective of co-infection with tuberculosisFunsho J. Ogunshola0Ruhul A. Khan1Musie Ghebremichael2Ragon Institute of MGH, MIT, and HarvardDepartment of Mathematics, University of ArizonaRagon Institute of MGH, MIT, and HarvardAbstract Background Immune reconstitution following the initiation of combination antiretroviral therapy (cART) significantly impacts the prognosis of individuals infected with human immunodeficiency virus (HIV). Our previous studies have indicated that the baseline CD4+ T cells count and percentage before cART initiation are predictors of immune recovery in TB-negative children infected with HIV, with TB co-infection potentially causing a delay in immune recovery. However, it remains unclear whether these predictors consistently impact immune reconstitution during long-term intensive cART treatment in TB-negative/positive children infected with HIV. Results We confirmed that the baseline CD4+ T cell count is a significant predictor of immune recovery following long-term intensive cART treatment among children aged 0 to 13 years. Children with lower CD4+ T cell count prior cART initiation did not show substantial immunological recovery during the follow-up period. Interestingly, children who were co-infected with TB and had higher baseline CD4+ T cell count eventually achieved good immunological recovery comparable to the TB-negative HIV-infected children. Hence, the baseline CD4+ T cell count at the onset of treatment serves as a reliable predictor of immunological reconstitution in HIV-infected children with or without TB co-infection. Taken together, this follow-up study validates our previous findings and further establishes that initiating cART early alongside early HIV testing can help prevent the diminished CD4+ T cell count associated with inadequate immunological reconstitution.https://doi.org/10.1186/s13104-024-07032-yHIVTBImmune recoveryCD4+ T cell countCART initiationPiecewise linear and mixed-effects models
spellingShingle Funsho J. Ogunshola
Ruhul A. Khan
Musie Ghebremichael
The prognosis for delayed immune recovery in HIV-infected children might be associated with pre-cART CD4+ T cell count irrespective of co-infection with tuberculosis
BMC Research Notes
HIV
TB
Immune recovery
CD4+ T cell count
CART initiation
Piecewise linear and mixed-effects models
title The prognosis for delayed immune recovery in HIV-infected children might be associated with pre-cART CD4+ T cell count irrespective of co-infection with tuberculosis
title_full The prognosis for delayed immune recovery in HIV-infected children might be associated with pre-cART CD4+ T cell count irrespective of co-infection with tuberculosis
title_fullStr The prognosis for delayed immune recovery in HIV-infected children might be associated with pre-cART CD4+ T cell count irrespective of co-infection with tuberculosis
title_full_unstemmed The prognosis for delayed immune recovery in HIV-infected children might be associated with pre-cART CD4+ T cell count irrespective of co-infection with tuberculosis
title_short The prognosis for delayed immune recovery in HIV-infected children might be associated with pre-cART CD4+ T cell count irrespective of co-infection with tuberculosis
title_sort prognosis for delayed immune recovery in hiv infected children might be associated with pre cart cd4 t cell count irrespective of co infection with tuberculosis
topic HIV
TB
Immune recovery
CD4+ T cell count
CART initiation
Piecewise linear and mixed-effects models
url https://doi.org/10.1186/s13104-024-07032-y
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