Impact of pre-existing dengue immunity on human antibody and memory B cell responses to Zika

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作者
Paulina Andrade
Ciara Gimblet-Ochieng
Faraz Modirian
Matthew Collins
Maritza Cárdenas
Leah C. Katzelnick
Magelda Montoya
Daniela Michlmayr
Guillermina Kuan
Angel Balmaseda
Josefina Coloma
Aravinda M. de Silva
Eva Harris
机构
[1] University of California,Division of Infectious Diseases and Vaccinology, School of Public Health
[2] Berkeley,Department of Microbiology and Immunology
[3] Colegio de Ciencias Biológicas y Ambientales,Laboratorio Nacional de Virología
[4] Universidad San Francisco de Quito,Hope Clinic of the Emory Vaccine Center, Division of Infectious Diseases, Department of Medicine, School of Medicine
[5] University of North Carolina,undefined
[6] Centro de Salud Sócrates Flores Vivas,undefined
[7] Ministry of Health,undefined
[8] Sustainable Sciences Institute,undefined
[9] Centro Nacional de Diagnóstico y Referencia,undefined
[10] Ministry of Health,undefined
[11] Emory University,undefined
来源
Nature Communications | / 10卷
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摘要
Little is known about enduring memory B cell (MBC) responses to Zika virus (ZIKV) and their relationship with circulating antibodies. Here we comprehensively assess MBC frequency and specificity alongside serum binding and neutralizing antibody responses to ZIKV ~2 weeks and ~8 months postinfection in 31 pediatric subjects with 0, 1 or >1 prior infections with the related dengue virus (DENV). ZIKV infection elicits a robust type-specific MBC response, and the majority of late convalescent anti-ZIKV serum neutralizing activity is attributable to ZIKV-specific antibodies. The number of prior DENV infections does not influence type-specific or cross-reactive MBC responses, although ZIKV has the highest cross-reactivity with DENV3. DENV cross-reactive MBCs expanded by ZIKV infection decline in number and proportion by late convalescence. Finally, ZIKV induces greater cross-reactivity in the MBC pool than in serum antibodies. Our data suggest immunity to DENV only modestly shapes breadth and magnitude of enduring ZIKV antibody responses.
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