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Craig Innes

Biographic Data

ID9070150
NAMECraig Innes
GIVEN NAMESCraig
FAMILY NAMEInnes
SIGNATUREINNES C
AFFILIATIONSAurum Institute
ORCID0000-0002-6872-5687
VERIFIEDNo
TOTAL WORKS2
TOTAL CITATIONS0
WORKS AS AUTHOR2
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2024
LATEST PUBLICATION YEAR2024
H-INDEX0
  • Safety and immunogenicity after a 30-month boost of a subtype C Alvac-HIV (vCP2438) vaccine prime plus bivalent subtype C gp120/MF59 vaccine boost (HVTN 100)

    Open Access•Vimla Naicker, Fatima Laher et al.•ARTICLE•PLOS Global Public Health•2024

    Induction of broad, durable immune responses is a challenge in HIV vaccine development. HVTN 100 Part A administered subtype C-containing ALVAC-HIV at months 0 and 1, and ALVAC-HIV with bivalent subtype C gp120/MF59 at months 3, 6 and 12. As IgG binding antibody and T-cell responses were similar or greater at month 12.5 vs. month 6.5, but waned by month 18, we investigated vaccine-elicited immune responses after a month 30 boost in this study, HV…

  • Safety, effectiveness and immunogenicity of heterologous mRNA-1273 boost after prime with Ad26.COV2.S among healthcare workers in South Africa

    Open Access•Nigel Garrett, Tarylee Reddy et al.•ARTICLE•PLOS Global Public Health•2024

    Limited studies have been conducted on the safety and effectiveness of heterologous COVID-19 vaccine boosting in lower income settings, especially those with high-HIV prevalence., The Sisonke Heterologous mRNA-1273 boost after prime with Ad26.COV2.S (SHERPA) trial evaluated a mRNA-1273 boost after Ad26.COV2.S priming in South Africa. SHERPA was a single-arm, open-label, phase 3 study nested in the Sisonke implementation trial of 500000 healthcare…

No prominent works on this page.

  • Safety and immunogenicity after a 30-month boost of a subtype C Alvac-HIV (vCP2438) vaccine prime plus bivalent subtype C gp120/MF59 vaccine boost (HVTN 100)

    Open Access•Vimla Naicker, Fatima Laher et al.•ARTICLE•PLOS Global Public Health•2024

    Induction of broad, durable immune responses is a challenge in HIV vaccine development. HVTN 100 Part A administered subtype C-containing ALVAC-HIV at months 0 and 1, and ALVAC-HIV with bivalent subtype C gp120/MF59 at months 3, 6 and 12. As IgG binding antibody and T-cell responses were similar or greater at month 12.5 vs. month 6.5, but waned by month 18, we investigated vaccine-elicited immune responses after a month 30 boost in this study, HV…

  • Safety, effectiveness and immunogenicity of heterologous mRNA-1273 boost after prime with Ad26.COV2.S among healthcare workers in South Africa

    Open Access•Nigel Garrett, Tarylee Reddy et al.•ARTICLE•PLOS Global Public Health•2024

    Limited studies have been conducted on the safety and effectiveness of heterologous COVID-19 vaccine boosting in lower income settings, especially those with high-HIV prevalence., The Sisonke Heterologous mRNA-1273 boost after prime with Ad26.COV2.S (SHERPA) trial evaluated a mRNA-1273 boost after Ad26.COV2.S priming in South Africa. SHERPA was a single-arm, open-label, phase 3 study nested in the Sisonke implementation trial of 500000 healthcare…

Immunology (2 works) · Medicine (2 works) · Adverse effect (1 work) · Antibody (1 work) · Antigen (1 work) · Booster dose (1 work) · Chemistry (1 work) · Clinical endpoint (1 work) · Clinical trial (1 work) · COVID-19 Clinical Research Studies (1 work)

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