Potent Neutralization Ability of a Human Monoclonal Antibody Against Serotype 1 Dengue Virus

被引:4
作者
Lu, Jiansheng [1 ]
Wang, Rong [1 ]
Xia, Binghui [1 ]
Yu, Yunzhou [1 ]
Zhou, Xiaowei [1 ]
Yang, Zhixin [1 ]
Huang, Peitang [1 ]
机构
[1] Beijing Inst Biotechnol, Lab Prot Engn, Beijing, Peoples R China
关键词
human monoclonal antibody; 1G5; dengue virus serotype 1; envelope protein; antibody-dependent enhancement; antibody neutralization; single plasma cells; MEMORY B-CELLS; COMPLETE GENOME SEQUENCE; ENVELOPE PROTEIN; DOMAIN-III; INFECTION; GLYCOPROTEIN; EPITOPES; FUSION; CHINA; ENHANCEMENT;
D O I
10.3389/fmicb.2018.01214
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The incidence of dengue virus (DENV) infections has been escalating in tropical and subtropical countries, but there are still no effective therapeutic options. In the present study, a DENV-1-specific human monoclonal antibody (HMAb), 1G5, isolated from single plasma cells obtained from the peripheral blood mononuclear cells of dengue patients was found to have potent neutralization activity against serotype 1 DENV (DENV-1). Its neutralization activity against DENV-2 was not as strong, and it was almost absent for DENV-3 and DENV-4. The results showed that HMAb 1G5 only binds to the envelop protein of intact DENV-1 or the envelop protein under unheated and non-reducing conditions, and that it does not bind to recombinant envelope protein. This could mean that the antibody recognizes a conformational epitope of the envelope protein. Further, the findings showed that HMAb 1G5 potently neutralizes DENV-1 in both the pre-and post-attachment phases of the virus at low concentrations. In vivo studies showed that HMAb 1G5 provides protection from DENV-1 infection in a murine model. In addition, antibody-dependent enhancement that occurs at lower doses of the antibody was completely abrogated by the introduction of Leu-to-Ala mutations (1G5-LALA) or deletion of nine amino acids (1G5-9del) in the Fc region. Therefore, HMAb 1G5 shows promise as a safe and effective agent for prophylactic and therapeutic treatment of DENV-1 infection.
引用
收藏
页数:10
相关论文
共 49 条
[1]   EPSTEIN-BARR VIRUS SUSCEPTIBILITY OF NORMAL HUMAN B-LYMPHOCYTE POPULATIONS [J].
AMAN, P ;
EHLINHENRIKSSON, B ;
KLEIN, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1984, 159 (01) :208-220
[2]   The Human Immune Response to Dengue Virus Is Dominated by Highly Cross-Reactive Antibodies Endowed with Neutralizing and Enhancing Activity [J].
Beltramello, Martina ;
Williams, Katherine L. ;
Simmons, Cameron P. ;
Macagno, Annalisa ;
Simonelli, Luca ;
Quyen, Nguyen Than Ha ;
Sukupolvi-Petty, Soila ;
Navarro-Sanchez, Erika ;
Young, Paul R. ;
de Silva, Aravinda M. ;
Rey, Felix A. ;
Varani, Luca ;
Whitehead, Stephen S. ;
Diamond, Michael S. ;
Harris, Eva ;
Lanzavecchia, Antonio ;
Sallusto, Federica .
CELL HOST & MICROBE, 2010, 8 (03) :271-283
[3]   The global distribution and burden of dengue [J].
Bhatt, Samir ;
Gething, Peter W. ;
Brady, Oliver J. ;
Messina, Jane P. ;
Farlow, Andrew W. ;
Moyes, Catherine L. ;
Drake, John M. ;
Brownstein, John S. ;
Hoen, Anne G. ;
Sankoh, Osman ;
Myers, Monica F. ;
George, Dylan B. ;
Jaenisch, Thomas ;
Wint, G. R. William ;
Simmons, Cameron P. ;
Scott, Thomas W. ;
Farrar, Jeremy J. ;
Hay, Simon I. .
NATURE, 2013, 496 (7446) :504-507
[4]   HUMAN MONOCLONAL-ANTIBODIES PRODUCED BY PRIMARY INVITRO IMMUNIZATION OF PERIPHERAL-BLOOD LYMPHOCYTES [J].
BORREBAECK, CAK ;
DANIELSSON, L ;
MOLLER, SA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (11) :3995-3999
[5]  
Chau Tran Nguyen Bich, 2008, J Infect Dis, V198, P516, DOI 10.1086/590117
[6]   The envelope glycoprotein domain III of dengue virus serotypes 1 and 2 inhibit virus entry [J].
Chin, J. F. L. ;
Chu, J. J. H. ;
Ng, M. L. .
MICROBES AND INFECTION, 2007, 9 (01) :1-6
[7]   Mechanistic Study of Broadly Neutralizing Human Monoclonal Antibodies against Dengue Virus That Target the Fusion Loop [J].
Costin, Joshua M. ;
Zaitseva, Elena ;
Kahle, Kristen M. ;
Nicholson, Cindo O. ;
Rowe, Dawne K. ;
Graham, Amanda S. ;
Bazzone, Lindsey E. ;
Hogancamp, Greg ;
Sierra, Marielys Figueroa ;
Fong, Rachel H. ;
Yang, Sung-Tae ;
Lin, Li ;
Robinson, James E. ;
Doranz, Benjamin J. ;
Chernomordik, Leonid V. ;
Michael, Scott F. ;
Schieffelin, John S. ;
Isern, Sharon .
JOURNAL OF VIROLOGY, 2013, 87 (01) :52-66
[8]  
CRAIN MJ, 1989, J IMMUNOL, V143, P1543
[9]   Identification of human neutralizing antibodies that bind to complex epitopes on dengue virions [J].
de Alwis, Ruklanthi ;
Smith, Scott A. ;
Olivarez, Nicholas P. ;
Messer, William B. ;
Huynh, Jeremy P. ;
Wahala, Wahala M. P. B. ;
White, Laura J. ;
Diamond, Michael S. ;
Baric, Ralph S. ;
Crowe, James E., Jr. ;
de Silva, Aravinda M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (19) :7439-7444
[10]   A new class of highly potent, broadly neutralizing antibodies isolated from viremic patients infected with dengue virus [J].
Dejnirattisai, Wanwisa ;
Wongwiwat, Wiyada ;
Supasa, Sunpetchuda ;
Zhang, Xiaokang ;
Dai, Xinghong ;
Rouvinsky, Alexander ;
Jumnainsong, Amonrat ;
Edwards, Carolyn ;
Nguyen Than Ha Quyen ;
Duangchinda, Thaneeya ;
Grimes, Jonathan M. ;
Tsai, Wen-Yang ;
Lai, Chih-Yun ;
Wang, Wei-Kung ;
Malasit, Prida ;
Farrar, Jeremy ;
Simmons, Cameron P. ;
Zhou, Z. Hong ;
Rey, Felix A. ;
Mongkolsapaya, Juthathip ;
Screaton, Gavin R. .
NATURE IMMUNOLOGY, 2015, 16 (02) :170-+