T-cell immune response after mRNA SARS-CoV-2 vaccines is frequently detected also in the absence of seroconversion in patients with lymphoid malignancies.
T-cell immune response after mRNA SARS-CoV-2 vaccines is frequently detected also in the absence of seroconversion in patients with lymphoid malignancies.
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DOI:
10.1111/bjh.17877
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发表时间:
2022-03
影响因子:
6.5
通讯作者:
Corradini P
中科院分区:
文献类型:
--
作者:
Marasco V;Carniti C;Guidetti A;Farina L;Magni M;Miceli R;Calabretta L;Verderio P;Ljevar S;Serpenti F;Morelli D;Apolone G;Ippolito G;Agrati C;Corradini P
Patients affected by lymphoid malignancies (LM) are frequently immune‐compromised, suffering increased mortality from COVID‐19. This prospective study evaluated serological and T‐cell responses after complete mRNA vaccination in 263 patients affected by chronic lymphocytic leukaemia, B‐ and T‐cell lymphomas and multiple myeloma. Results were compared with those of 167 healthy subjects matched for age and sex. Overall, patient seroconversion rate was 64·6%: serological response was lower in those receiving anti‐cancer treatments in the 12 months before vaccination: 55% vs 81·9% (P < 0·001). Anti‐CD20 antibody plus chemotherapy treatment was associated with the lowest seroconversion rate: 17·6% vs. 71·2% (P < 0·001). In the multivariate analysis conducted in the subgroup of patients on active treatment, independent predictors for seroconversion were: anti‐CD20 treatment (P < 0·001), aggressive B‐cell lymphoma diagnosis (P = 0·002), and immunoglobulin M levels <40 mg/dl (P = 0·030). The T‐cell response was evaluated in 99 patients and detected in 85 of them (86%). Of note, 74% of seronegative patients had a T‐cell response, but both cellular and humoral responses were absent in 13·1% of cases. Our findings raise some concerns about the protection that patients with LM, particularly those receiving anti‐CD20 antibodies, may gain from vaccination. These patients should strictly maintain all the protective measures.
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DOI:
10.1056/nejmoa2034577
发表时间:
2020-12-31
期刊:
The New England journal of medicine
影响因子:
--
作者:
Polack FP;Thomas SJ;Kitchin N;Absalon J;Gurtman A;Lockhart S;Perez JL;Pérez Marc G;Moreira ED;Zerbini C;Bailey R;Swanson KA;Roychoudhury S;Koury K;Li P;Kalina WV;Cooper D;Frenck RW Jr;Hammitt LL;Türeci Ö;Nell H;Schaefer A;Ünal S;Tresnan DB;Mather S;Dormitzer PR;Şahin U;Jansen KU;Gruber WC;C4591001 Clinical Trial Group
通讯作者:
C4591001 Clinical Trial Group
DOI:
10.1158/1078-0432.ccr-11-1221
发表时间:
2012-03-01
期刊:
Clinical cancer research : an official journal of the American Association for Cancer Research
影响因子:
--
作者:
Noonan K;Rudraraju L;Ferguson A;Emerling A;Pasetti MF;Huff CA;Borrello I
通讯作者:
Borrello I
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:
4.5
作者:
Agrati C;Castilletti C;Goletti D;Meschi S;Sacchi A;Matusali G;Bordoni V;Petrone L;Lapa D;Notari S;Vanini V;Colavita F;Aiello A;Agresta A;Farroni C;Grassi G;Leone S;Vaia F;Capobianchi MR;Ippolito G;Puro V;On Behalf Of The Inmi Covid-Vaccine Study Group
通讯作者:
On Behalf Of The Inmi Covid-Vaccine Study Group
影响因子:
56.3
作者:
Cordonnier, Catherine;Einarsdottir, Sigrun;Wenneras, Christine
通讯作者:
Wenneras, Christine