Neutralization breadth of SARS-CoV-2 viral variants following primary series and booster SARS-CoV-2 vaccines in patients with cancer.
Neutralization breadth of SARS-CoV-2 viral variants following primary series and booster SARS-CoV-2 vaccines in patients with cancer.
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DOI:
10.1016/j.ccell.2021.12.002
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发表时间:
2022-01-10
期刊:
影响因子:
50.3
通讯作者:
CANVAX team
中科院分区:
文献类型:
--
作者:
Naranbhai V;St Denis KJ;Lam EC;Ofoman O;Garcia-Beltran WF;Mairena CB;Bhan AK;Gainor JF;Balazs AB;Iafrate AJ;CANVAX team
Patients with cancer are more likely to have impaired immune responses to SARS-CoV-2 vaccines. We study the breadth of responses against SARS-CoV-2 variants after primary vaccination in 178 patients with a variety of tumor types and after booster doses in a subset. Neutralization of alpha, beta, gamma, and delta SARS-CoV-2 variants is impaired relative to wildtype, regardless of vaccine type. Regardless of viral variant, mRNA1273 is the most immunogenic, followed by BNT162b2, and then Ad26.COV2.S. Neutralization of more variants (breadth) is associated with a greater magnitude of wildtype neutralization, and increases with time since vaccination; advancing age associates with a lower breadth. The concentrations of anti-spike protein antibody are a good surrogate for breadth (positive predictive value of =90% at >1,000 U/mL). Booster SARS-CoV-2 vaccines confer enhanced breadth. These data suggest that achieving a high antibody titer is desirable to achieve broad neutralization; a single booster dose with the current vaccines increases the breadth of responses against variants. Naranbhai et al. examine how well current wildtype-based SARS-CoV-2 vaccines perform in patients with cancer in neutralizing viral variants. The findings support preferring the most immunogenic wildtype vaccines (i.e., mRNA1273 or BNT162b2) for patients at high risk to generate breadth against variants.
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DOI:
10.1093/infdis/jiab593
发表时间:
2022-04-01
期刊:
The Journal of infectious diseases
影响因子:
--
作者:
Naranbhai V;Garcia-Beltran WF;Chang CC;Berrios Mairena C;Thierauf JC;Kirkpatrick G;Onozato ML;Cheng J;St Denis KJ;Lam EC;Kaseke C;Tano-Menka R;Yang D;Pavlovic M;Yang W;Kui A;Miller TE;Astudillo MG;Cahill JE;Dighe AS;Gregory DJ;Poznansky MC;Gaiha GD;Balazs AB;Iafrate AJ
通讯作者:
Iafrate AJ
DOI:
10.1016/s2352-3026(21)00110-1
发表时间:
2021-06
期刊:
The Lancet. Haematology
影响因子:
--
作者:
Bird S;Panopoulou A;Shea RL;Tsui M;Saso R;Sud A;West S;Smith K;Barwood J;Kaczmarek E;Panlaqui C;Kaiser M;Stern S;Pawlyn C;Boyd K
通讯作者:
Boyd K
影响因子:
64.5
作者:
Garcia-Beltran, Wilfredo F.;Lam, Evan C.;Balazs, Alejandro B.
通讯作者:
Balazs, Alejandro B.
影响因子:
50.3
作者:
Thakkar A;Gonzalez-Lugo JD;Goradia N;Gali R;Shapiro LC;Pradhan K;Rahman S;Kim SY;Ko B;Sica RA;Kornblum N;Bachier-Rodriguez L;McCort M;Goel S;Perez-Soler R;Packer S;Sparano J;Gartrell B;Makower D;Goldstein YD;Wolgast L;Verma A;Halmos B
通讯作者:
Halmos B
影响因子:
64.8
作者:
Cho A;Muecksch F;Schaefer-Babajew D;Wang Z;Finkin S;Gaebler C;Ramos V;Cipolla M;Mendoza P;Agudelo M;Bednarski E;DaSilva J;Shimeliovich I;Dizon J;Daga M;Millard KG;Turroja M;Schmidt F;Zhang F;Tanfous TB;Jankovic M;Oliveria TY;Gazumyan A;Caskey M;Bieniasz PD;Hatziioannou T;Nussenzweig MC
通讯作者:
Nussenzweig MC