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Effectiveness of ChAdOx1 nCoV-19 vaccine against SARS-CoV-2 infection during the delta (B.1.617.2) variant surge in India: a test-negative, case-control study and a mechanistic study of post-vaccination immune responses.
Thiruvengadam, Ramachandran; Awasthi, Amit; Medigeshi, Guruprasad; Bhattacharya, Sankar; Mani, Shailendra; Sivasubbu, Sridhar; Shrivastava, Tripti; Samal, Sweety; Rathna Murugesan, Deepika; Koundinya Desiraju, Bapu; Kshetrapal, Pallavi; Pandey, Rajesh; Scaria, Vinod; Kumar Malik, Praveen; Taneja, Juhi; Binayke, Akshay; Vohra, Tarini; Zaheer, Aymaan; Rathore, Deepak; Ahmad Khan, Naseem; Shaman, Heena; Ahmed, Shubbir; Kumar, Rajesh; Deshpande, Suprit; Subramani, Chandru; Wadhwa, Nitya; Gupta, Nimesh; Pandey, Anil K; Bhattacharya, Jayanta; Agrawal, Anurag; Vrati, Sudhanshu; Bhatnagar, Shinjini; Garg, Pramod Kumar.
  • Thiruvengadam R; Translational Health Science and Technology Institute, Faridabad, India.
  • Awasthi A; Translational Health Science and Technology Institute, Faridabad, India.
  • Medigeshi G; Translational Health Science and Technology Institute, Faridabad, India.
  • Bhattacharya S; Translational Health Science and Technology Institute, Faridabad, India.
  • Mani S; Translational Health Science and Technology Institute, Faridabad, India.
  • Sivasubbu S; Council of Scientific and Industrial Research-Institute of Genomics and Integrative Biology, New Delhi, India.
  • Shrivastava T; Translational Health Science and Technology Institute, Faridabad, India.
  • Samal S; Translational Health Science and Technology Institute, Faridabad, India.
  • Rathna Murugesan D; Translational Health Science and Technology Institute, Faridabad, India.
  • Koundinya Desiraju B; Translational Health Science and Technology Institute, Faridabad, India.
  • Kshetrapal P; Translational Health Science and Technology Institute, Faridabad, India.
  • Pandey R; Council of Scientific and Industrial Research-Institute of Genomics and Integrative Biology, New Delhi, India.
  • Scaria V; Council of Scientific and Industrial Research-Institute of Genomics and Integrative Biology, New Delhi, India.
  • Kumar Malik P; ESIC Medical College and Hospital, Faridabad, India.
  • Taneja J; ESIC Medical College and Hospital, Faridabad, India.
  • Binayke A; Translational Health Science and Technology Institute, Faridabad, India.
  • Vohra T; Translational Health Science and Technology Institute, Faridabad, India.
  • Zaheer A; Translational Health Science and Technology Institute, Faridabad, India.
  • Rathore D; Translational Health Science and Technology Institute, Faridabad, India.
  • Ahmad Khan N; Translational Health Science and Technology Institute, Faridabad, India.
  • Shaman H; Translational Health Science and Technology Institute, Faridabad, India.
  • Ahmed S; Translational Health Science and Technology Institute, Faridabad, India.
  • Kumar R; Translational Health Science and Technology Institute, Faridabad, India.
  • Deshpande S; Translational Health Science and Technology Institute, Faridabad, India.
  • Subramani C; Regional Centre for Biotechnology, Faridabad, India.
  • Wadhwa N; Translational Health Science and Technology Institute, Faridabad, India.
  • Gupta N; National Institute of Immunology, Delhi, India.
  • Pandey AK; ESIC Medical College and Hospital, Faridabad, India.
  • Bhattacharya J; Translational Health Science and Technology Institute, Faridabad, India; International AIDS Vaccine Initiative, New Delhi, India.
  • Agrawal A; Council of Scientific and Industrial Research-Institute of Genomics and Integrative Biology, New Delhi, India.
  • Vrati S; Regional Centre for Biotechnology, Faridabad, India.
  • Bhatnagar S; Translational Health Science and Technology Institute, Faridabad, India.
  • Garg PK; Translational Health Science and Technology Institute, Faridabad, India. Electronic address: pgarg@thsti.res.in.
Lancet Infect Dis ; 22(4): 473-482, 2022 04.
Article in English | MEDLINE | ID: covidwho-1757985
ABSTRACT

BACKGROUND:

SARS-CoV-2 variants of concern (VOCs) have threatened COVID-19 vaccine effectiveness. We aimed to assess the effectiveness of the ChAdOx1 nCoV-19 vaccine, predominantly against the delta (B.1.617.2) variant, in addition to the cellular immune response to vaccination.

METHODS:

We did a test-negative, case-control study at two medical research centres in Faridabad, India. All individuals who had a positive RT-PCR test for SARS-CoV-2 infection between April 1, 2021, and May 31, 2021, were included as cases and individuals who had a negative RT-PCR test were included as controls after matching with cases on calendar week of RT-PCR test. The primary outcome was effectiveness of complete vaccination with the ChAdOx1 nCoV-19 vaccine against laboratory-confirmed SARS-CoV-2 infection. The secondary outcomes were effectiveness of a single dose against SARS-CoV-2 infection and effectiveness of a single dose and complete vaccination against moderate-to-severe disease among infected individuals. Additionally, we tested in-vitro live-virus neutralisation and T-cell immune responses to the spike protein of the wild-type SARS-CoV-2 and VOCs among healthy (anti-nucleocapsid antibody negative) recipients of the ChAdOx1 nCoV-19 vaccine.

FINDINGS:

Of 2379 cases of confirmed SARS-CoV-2 infection, 85 (3·6%) were fully vaccinated compared with 168 (8·5%) of 1981 controls (adjusted OR [aOR] 0·37 [95% CI 0·28-0·48]), giving a vaccine effectiveness against SARS-CoV-2 infection of 63·1% (95% CI 51·5-72·1). 157 (6·4%) of 2451 of cases and 181 (9·1%) of 1994) controls had received a single dose of the ChAdOx1 nCoV-19 vaccine (aOR 0·54 [95% CI 0·42-0·68]), thus vaccine effectiveness of a single dose against SARS-CoV-2 infection was 46·2% (95% CI 31·6-57·7). One of 84 cases with moderate-to-severe COVID-19 was fully vaccinated compared with 84 of 2295 cases with mild COVID-19 (aOR 0·19 [95% CI 0·01-0·90]), giving a vaccine effectiveness of complete vaccination against moderate-to-severe disease of 81·5% (95% CI 9·9-99·0). The effectiveness of a single dose against moderate-to-severe disease was 79·2% (95% CI 46·1-94·0); four of 87 individuals with moderate-to-severe COVID-19 had received a single dose compared with 153 of 2364 participants with mild disease (aOR 0·20 [95% CI 0·06-0·54]). Among 49 healthy, fully vaccinated individuals, neutralising antibody responses were lower against the alpha (B.1.1.7; geometric mean titre 244·7 [95% CI 151·8-394·4]), beta (B.1.351; 97·6 [61·2-155·8]), kappa (B.1.617.1; 112·8 [72·7-175·0]), and delta (88·4 [61·2-127·8]) variants than against wild-type SARS-CoV-2 (599·4 [376·9-953·2]). However, the antigen-specific CD4 and CD8 T-cell responses were conserved against both the delta variant and wild-type SARS-CoV-2.

INTERPRETATION:

The ChAdOx1 nCoV-19 vaccine remained effective against moderate-to-severe COVID-19, even during a surge that was dominated by the highly transmissible delta variant of SARS-CoV-2. Spike-specific T-cell responses were maintained against the delta variant. Such cellular immune protection might compensate for waning humoral immunity.

FUNDING:

Department of Biotechnology India, Council of Scientific and Industrial Research India, and Fondation Botnar.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Humans Language: English Journal: Lancet Infect Dis Journal subject: Communicable Diseases Year: 2022 Document Type: Article Affiliation country: S1473-3099(21)00680-0

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Humans Language: English Journal: Lancet Infect Dis Journal subject: Communicable Diseases Year: 2022 Document Type: Article Affiliation country: S1473-3099(21)00680-0