Attenuated immunogenicity of SARS-CoV-2 vaccines and risk factors in stem cell transplant recipients: a meta-analysis

dc.contributor.authorMeejun T.
dc.contributor.authorSrisurapanont K.
dc.contributor.authorManothummetha K.
dc.contributor.authorThongkam A.
dc.contributor.authorMejun N.
dc.contributor.authorChuleerarux N.
dc.contributor.authorSanguankeo A.
dc.contributor.authorPhongkhun K.
dc.contributor.authorLeksuwankun S.
dc.contributor.authorThanakitcharu J.
dc.contributor.authorLerttiendamrong B.
dc.contributor.authorLangsiri N.
dc.contributor.authorTorvorapanit P.
dc.contributor.authorWorasilchai N.
dc.contributor.authorPlongla R.
dc.contributor.authorHirankarn N.
dc.contributor.authorNematollahi S.
dc.contributor.authorPermpalung N.
dc.contributor.authorMoonla C.
dc.contributor.authorKates O.S.
dc.contributor.otherMahidol University
dc.date.accessioned2023-10-19T18:01:58Z
dc.date.available2023-10-19T18:01:58Z
dc.date.issued2023-09-26
dc.description.abstractImmunogenicity of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination is diminished in hematopoietic stem cell transplant (HSCT) recipients. To summarize current evidence and identify risk factors for attenuated responses, 5 electronic databases were searched since database inceptions through 12 January 2023 for studies reporting humoral and/or cellular immunogenicity of SARS-CoV-2 vaccination in the HSCT population. Using descriptive statistics and random-effects models, extracted numbers of responders and pooled odds ratios (pORs) with 95% confidence intervals (CIs) for risk factors of negative immune responses were analyzed (PROSPERO: CRD42021277109). From 61 studies with 5906 HSCT recipients, after 1, 2, and 3 doses of messenger RNA (mRNA) SARS-CoV-2 vaccines, the mean antispike antibody seropositivity rates (95% CI) were 38% (19-62), 81% (77-84), and 80% (75-84); neutralizing antibody seropositivity rates were 52% (40-64), 71% (54-83), and 78% (61-89); and cellular immune response rates were 52% (39-64), 66% (51-79), and 72% (52-86). After 2 vaccine doses, risk factors (pOR; 95% CI) associated with antispike seronegativity were male recipients (0.63; 0.49-0.83), recent rituximab exposure (0.09; 0.03-0.21), haploidentical allografts (0.46; 0.22-0.95), <24 months from HSCT (0.25; 0.07-0.89), lymphopenia (0.18; 0.13-0.24), hypogammaglobulinemia (0.23; 0.10-0.55), concomitant chemotherapy (0.48; 0.29-0.78) and immunosuppression (0.18; 0.13-0.25). Complete remission of underlying hematologic malignancy (2.55; 1.05-6.17) and myeloablative conditioning (1.72; 1.30-2.28) compared with reduced-intensity conditioning were associated with antispike seropositivity. Ongoing immunosuppression (0.31; 0.10-0.99) was associated with poor cellular immunogenicity. In conclusion, attenuated humoral and cellular immune responses to mRNA SARS-CoV-2 vaccination are associated with several risk factors among HSCT recipients. Optimizing individualized vaccination and developing alternative COVID-19 prevention strategies are warranted.
dc.identifier.citationBlood Advances Vol.7 No.18 (2023) , 5624-5636
dc.identifier.doi10.1182/bloodadvances.2023010349
dc.identifier.eissn24739537
dc.identifier.issn24739529
dc.identifier.pmid37389818
dc.identifier.scopus2-s2.0-85173507363
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/90573
dc.rights.holderSCOPUS
dc.subjectMedicine
dc.titleAttenuated immunogenicity of SARS-CoV-2 vaccines and risk factors in stem cell transplant recipients: a meta-analysis
dc.typeReview
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85173507363&origin=inward
oaire.citation.endPage5636
oaire.citation.issue18
oaire.citation.startPage5624
oaire.citation.titleBlood Advances
oaire.citation.volume7
oairecerif.author.affiliationSiriraj Hospital
oairecerif.author.affiliationFaculty of Medicine, Chiang Mai University
oairecerif.author.affiliationUniversity of Miami
oairecerif.author.affiliationChulalongkorn University
oairecerif.author.affiliationKing Chulalongkorn Memorial Hospital
oairecerif.author.affiliationUniversity of Arizona College of Medicine – Tucson
oairecerif.author.affiliationFaculty of Medicine, Thammasat University
oairecerif.author.affiliationFaculty of Medicine, Srinakharinwirot University
oairecerif.author.affiliationFaculty of Medicine, Chulalongkorn University
oairecerif.author.affiliationJohns Hopkins School of Medicine

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