Vaccine-induced spike- and nucleocapsid-specific cellular responses maintain potent cross-reactivity to SARS-CoV-2 Delta and Omicron variants

被引:15
作者
Chiuppesi, Flavia [1 ,2 ]
Zaia, John A. [3 ]
Faircloth, Katelyn [1 ,2 ]
Johnson, Daisy [1 ,2 ]
Ly, Minh [1 ,2 ]
Karpinski, Veronica [1 ,2 ]
La Rosa, Corinna [1 ,2 ]
Drake, Jennifer [4 ]
Marcia, Joan [4 ]
Acosta, Ann Marie [4 ]
Dempsey, Shannon [1 ,2 ]
Taplitz, Randy A. [5 ,6 ]
Zhou, Qiao [1 ,2 ]
Park, Yoonsuh [1 ,2 ]
Francisco, Sandra Ortega [1 ,2 ]
Kaltcheva, Teodora [1 ,2 ]
Frankel, Paul H. [7 ]
Rosen, Steven [1 ,2 ]
Wussow, Felix [1 ,2 ]
Dadwal, Sanjeet [5 ,6 ]
Diamond, Don J. [1 ,2 ]
机构
[1] Dept Hematol & HCT, 1500 E Duarte Rd, Duarte, CA 91010 USA
[2] Hematol Malignancies Res Inst, 1500 E Duarte Rd, Duarte, CA 91010 USA
[3] City Hope Natl Med Ctr, Ctr Gene Therapy, Natl Med Ctr, 1500 E Duarte Rd, Duarte, CA 91010 USA
[4] City Hope Natl Med Ctr, Clin Trials Off, Natl Med Ctr, 1500 E Duarte Rd, Duarte, CA 91010 USA
[5] City Hope Natl Med Ctr, Div Infect Dis, Natl Med Ctr, 1500 E Duarte Rd, Duarte, CA 91010 USA
[6] City Hope Natl Med Ctr, Dept Med, Natl Med Ctr, 1500 E Duarte Rd, Duarte, CA 91010 USA
[7] City Hope Natl Med Ctr, Dept Biostat, Natl Med Ctr, 1500 E Duarte Rd, Duarte, CA 91010 USA
关键词
D O I
10.1016/j.isci.2022.104745
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cell-mediated immunity may contribute to providing protection against SARS-CoV-2 and its variants of concern (VOC). We developed COH04S1, a synthetic multiantigen modified vaccinia Ankara (MVA)-based COVID-19 vaccine that stimulated potent spike (S) and nucleocapsid (N) antigen-specific humoral and cellular immunity in a phase 1 clinical trial in healthy adults. Here, we show that individuals vaccinated with COH04S1 or mRNA vaccine BNT162b2 maintain robust crossreactive cellular immunity for six or more months post-vaccination. Although neutralizing antibodies induced in COH04S1- and BNT162b2-vaccinees showed reduced activity against Delta and Omicron varLnts compared to ancestral SARS-CoV-2, S-specific T cells elicited in both COK04S1- and BNT162b2-vaccinees and N-specific T cells elicited in COH0451-vaccinees demonstrated potent and equivalent cross-reactivity against ancestral SARS-CoV-2 and the major VOC. These results suggest that vaccine-induced T cells to S and N antigens may constitute a critical second line of defense to provide long-term protection against SARS-CoV-2 VOC.
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页数:15
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