Evaluation of conserved and variable influenza antigens for immunization against different isolates of H5N1 viruses Export

@article{citeulike:4545226, abstract = {The combination of rapid evolution and high mortality in human cases of infections has raised concerns that the H5N1 avian influenza virus may become a new, possibly severe, pandemic virus. Vaccination is likely to be the most efficient strategy to mitigate the impact of the next influenza pandemic. The present study evaluates B and T cell immune responses generated by the H5N1 viral antigens, hemagglutinin (HA), neuraminidase (NA), nucleoprotein (NP), or the M2 ion channel in parallel, expressed from a DNA vaccine vehicle. Protection studies of immunized mice challenged with 100 LD50 of homologous or heterologous H5N1 viruses indicate that HA afforded better protection than the NA, NP or M2 DNA vaccines. The antibody response was also higher in HA-vaccinated mice as determined by hemagglutination inhibition (HI) and neutralizing antibodies (NAB) assays. Interestingly, the T cell response was higher against HA than against NA, NP or M2 and was detectable at low doses of the DNA–HA vaccine capable of inducing complete protection, despite the absence of a detectable B cell response. This study emphasizes the need to evaluate the relationship between both arms of the adaptive immune responses in regards to protective efficacy against influenza virus.}, author = {Patel, Ami and Tran, Kaylie and Gray, Michael and Li, Yan and Ao, Zhujun and Yao, Xiaojian and Kobasa, Darwyn and Kobinger, Gary P.}, citeulike-article-id = {4545226}, citeulike-linkout-0 = {http://dx.doi.org/10.1016/j.vaccine.2009.03.023}, citeulike-linkout-1 = {http://linkinghub.elsevier.com/retrieve/pii/S0264410X0900406X}, day = {18}, doi = {10.1016/j.vaccine.2009.03.023}, issn = {0264410X}, journal = {Vaccine}, keywords = {antibody, antigen, influenza}, month = {May}, number = {23}, pages = {3083--3089}, posted-at = {2009-05-19 15:57:53}, priority = {2}, title = {Evaluation of conserved and variable influenza antigens for immunization against different isolates of H5N1 viruses}, url = {http://dx.doi.org/10.1016/j.vaccine.2009.03.023}, volume = {27}, year = {2009} }

TY - JOUR ID - citeulike:4545226 L3 - citeulike-article-id:4545226 N2 - The combination of rapid evolution and high mortality in human cases of infections has raised concerns that the H5N1 avian influenza virus may become a new, possibly severe, pandemic virus. Vaccination is likely to be the most efficient strategy to mitigate the impact of the next influenza pandemic. The present study evaluates B and T cell immune responses generated by the H5N1 viral antigens, hemagglutinin (HA), neuraminidase (NA), nucleoprotein (NP), or the M2 ion channel in parallel, expressed from a DNA vaccine vehicle. Protection studies of immunized mice challenged with 100 LD50 of homologous or heterologous H5N1 viruses indicate that HA afforded better protection than the NA, NP or M2 DNA vaccines. The antibody response was also higher in HA-vaccinated mice as determined by hemagglutination inhibition (HI) and neutralizing antibodies (NAB) assays. Interestingly, the T cell response was higher against HA than against NA, NP or M2 and was detectable at low doses of the DNA–HA vaccine capable of inducing complete protection, despite the absence of a detectable B cell response. This study emphasizes the need to evaluate the relationship between both arms of the adaptive immune responses in regards to protective efficacy against influenza virus. IS - 23 JF - Vaccine SN - 0264410X EP - 3089 TI - Evaluation of conserved and variable influenza antigens for immunization against different isolates of H5N1 viruses VL - 27 SP - 3083 KW - antibody KW - antigen KW - influenza AU - Patel, Ami AU - Tran, Kaylie AU - Gray, Michael AU - Li, Yan AU - Ao, Zhujun AU - Yao, Xiaojian AU - Kobasa, Darwyn AU - Kobinger, Gary PY - 2009/05/18/ UR - http://dx.doi.org/10.1016/j.vaccine.2009.03.023 ER -