Passive Protection Assay of Monoclonal Antibodies Against Dengue Virus in Suckling Mice

被引:4
作者
Chen, Zongtao [1 ]
Liu, Li-Mei [2 ]
Gao, Na [1 ]
Xu, Xiao-Feng [1 ]
Zhang, Jun-Lei [1 ]
Wang, Jia-Li [1 ]
An, Jing [3 ]
机构
[1] Third Mil Med Univ, Dept Microbiol, Chongqing 400042, Peoples R China
[2] Third Mil Med Univ, Southwest Hosp, Inst Pathol, Chongqing 400042, Peoples R China
[3] Capital Med Univ, Sch Basic Med Sci, Dept Microbiol, Beijing 100069, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
ENVELOPE PROTEIN; INFECTION; VACCINE; IMMUNOGENICITY; DIAGNOSIS; BINDING; CELLS;
D O I
10.1007/s00284-009-9356-4
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Dengue fever and dengue hemorrhagic fever/dengue shock syndrome are highly infectious diseases caused by dengue virus (DV). Specific monoclonal antibodies (mAbs) against DV are vital for diagnosis, pathological studies, and passive immune therapy. In this study, purified DV serotype 2 (DV2) was used as antigen and BALB/c mice were immunized to induce specific antibodies. We established five hybridoma cell lines, called 78#, 1E7, 7F7, 8F12, and 8H1, respectively, and evaluated them by enzyme-linked immunosorbent assay, indirect immunofluorescence assay, Western blot, plaque reduction neutralization test, and suckling mice protection assay. Lines 78#, 1E7, 7F7, and 8F12 showed a neutralizing effect, and lines 78#, 1E7, 8F12, and 8H1 recognized envelope glycoprotein of DV2. Among them, lines 78# and 8F12 had stronger neutralizing ability in vitro and could protect some suckling mice from virus challenge. Our results demonstrate that immunization with purified virion is efficient for the production of specific neutralizing mAbs against DV2, and these mAbs could be useful tools for studying or treating DV infection.
引用
收藏
页码:326 / 331
页数:6
相关论文
共 20 条
[1]   Production and characterization of monoclonal antibody specific to recombinant dengue multi-epitope protein [J].
Abhyankar, Ajay Vinayak ;
Bhargava, Rakesh ;
Jana, Asha Mukul ;
Sahni, Ajay Kumar ;
Rao, P. V. Lakshmana .
HYBRIDOMA, 2008, 27 (03) :191-198
[2]   Mutational evidence for an internal fusion peptide in flavivirus envelope protein E [J].
Allison, SL ;
Schalich, J ;
Stiasny, K ;
Mandl, CW ;
Heinz, FX .
JOURNAL OF VIROLOGY, 2001, 75 (09) :4268-4275
[3]   Live attenuated tetravalent dengue vaccine [J].
Bhamarapravati, N ;
Sutee, Y .
VACCINE, 2000, 18 :44-47
[4]   Recombinant human polyclonal antibodies: A new class of therapeutic antibodies against viral infections [J].
Bregenholt, Soren ;
Jensen, Allan ;
Lantto, Johan ;
Hyldig, Sara ;
Haurum, John S. .
CURRENT PHARMACEUTICAL DESIGN, 2006, 12 (16) :2007-2015
[5]   Antibodies against West Nile virus nonstructural protein NS1 prevent lethal infection through Fc γ receptor-dependent and -independent mechanisms [J].
Chung, KM ;
Nybakken, GE ;
Thompson, BS ;
Engle, MJ ;
Marri, A ;
Fremont, DH ;
Diamond, MS .
JOURNAL OF VIROLOGY, 2006, 80 (03) :1340-1351
[6]   A human monoclonal antibody cocktail as a novel component of rabies postexposure prophylaxis [J].
de Kruif, John ;
Bakker, Alexander B. H. ;
Marissen, Wilfred E. ;
Kramer, R. Arjen ;
Throsby, Mark ;
Rupprecht, Charles E. ;
Goudsmit, Jaap .
ANNUAL REVIEW OF MEDICINE, 2007, 58 :359-368
[7]   RECOMBINANT VACCINIA VIRUSES CO-EXPRESSING DENGUE-1 GLYCOPROTEINS PRM AND E-INDUCE NEUTRALIZING ANTIBODIES IN MICE [J].
FONSECA, BAL ;
PINCUS, S ;
SHOPE, RE ;
PAOLETTI, E ;
MASON, PW .
VACCINE, 1994, 12 (03) :279-285
[8]   Precipitation of bovine rotavirus by polyethylen glycol (PEG) and its application to produce polyclonal and monoclonal antibodies [J].
Fontes, LVQ ;
Campos, GS ;
Beck, PA ;
Brandao, CFL ;
Sardi, SI .
JOURNAL OF VIROLOGICAL METHODS, 2005, 123 (02) :147-153
[9]   Dengue tetravalent DNA vaccine increases its immunogenicity in mice when mixed with a dengue type 2 subunit vaccine or an inactivated Japanese encephalitis vaccine [J].
Imoto, Jun-ichi ;
Konishi, Eiji .
VACCINE, 2007, 25 (06) :1076-1084
[10]   Evaluation of an NS1 antigen detection for diagnosis of acute dengue infection in patients with acute febrile illness [J].
Lapphra, Keswadee ;
Sangcharaswichai, Anyarit ;
Chokephaibulkit, Kulkanya ;
Tiengrim, Surapee ;
Piriyakarnsakul, Wirongrong ;
Chakorn, Tipa ;
Yoksan, Sutee ;
Wattanamongkolsil, Luksamee ;
Thamlikitkul, Visanu .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2008, 60 (04) :387-391