tetano
Editor, Senior Moderator
J Virol. 2018 Aug 1. pii: JVI.00969-18. doi: 10.1128/JVI.00969-18. [Epub ahead of print]
[h=1]Complement C3 Plays a Key Role in Inducing Humoral and Cellular Immune Responses to Influenza Virus Strain Specific HA or Cross Protective M2e vaccination.[/h] Kim YJ[SUP]1,[/SUP][SUP]2[/SUP], Kim KH[SUP]1[/SUP], Ko EJ[SUP]1,[/SUP][SUP]3[/SUP], Kim MC[SUP]1,[/SUP][SUP]4[/SUP], Lee YN[SUP]1,[/SUP][SUP]5[/SUP], Jung YJ[SUP]1[/SUP], Lee YT[SUP]1[/SUP], Kwon YM[SUP]1[/SUP], Song JM[SUP]6[/SUP], Kang SM[SUP]7[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] The complement pathway is involved in eliminating antigen immune complexes. However, the role of the C3 complement system remains largely unknown in influenza virus M2 extracellular (M2e) domain or hemagglutinin (HA) vaccine-mediated protection after vaccination. Using a C3 knockout (C3 KO) mouse model, we found that complement protein C3 was required for effective induction of immune responses to vaccination with M2e-based or HA-based vaccines, which include isotype class-switched antibodies and effector CD4 and CD8 T cell responses. C3 KO mice after active immunization with cross protective non-neutralizing M2e-based vaccine were not protected against influenza virus although low levels of M2e specific antibodies were protective after passive co-administration with virus in wild type mice. In contrast, C3 KO mice that were immunized with strain-specific neutralizing HA-based vaccine were protected against homologous virus challenge despite lower levels of HA antibody responses. C3 KO mice showed impaired maintenance of innate immune cells and a defect in innate immune responses upon exposure to antigens. The findings in this study suggest that C3 is required for effective induction of humoral and cellular adaptive immune responses as well as protective immunity after non-neutralizing influenza M2e vaccination.IMPORTANCEComplement is the well-known innate immune defense system by involving in the opsonization and lysis of pathogens but less studied in establishing adaptive immunity after vaccination. Influenza virus HA-based vaccination confers protection via strain-specific neutralizing antibodies whereas M2e-based vaccination induces a broad spectrum of protection by immunity against the conserved M2e epitopes. This study revealed the critical roles of C3 complement in inducing humoral and cellular immune responses after immunization with M2e or HA vaccines. C3 was found to be required for protection by M2e-based but not by HA-based active vaccination as well as for maintaining innate antigen presenting cells. Findings in this study have insight into better understanding the roles of C3 complement in inducing effective innate and adaptive immunity as well as in conferring protection by cross protective conserved M2e vaccination.
PMID: 30068650 DOI: 10.1128/JVI.00969-18
[h=1]Complement C3 Plays a Key Role in Inducing Humoral and Cellular Immune Responses to Influenza Virus Strain Specific HA or Cross Protective M2e vaccination.[/h] Kim YJ[SUP]1,[/SUP][SUP]2[/SUP], Kim KH[SUP]1[/SUP], Ko EJ[SUP]1,[/SUP][SUP]3[/SUP], Kim MC[SUP]1,[/SUP][SUP]4[/SUP], Lee YN[SUP]1,[/SUP][SUP]5[/SUP], Jung YJ[SUP]1[/SUP], Lee YT[SUP]1[/SUP], Kwon YM[SUP]1[/SUP], Song JM[SUP]6[/SUP], Kang SM[SUP]7[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] The complement pathway is involved in eliminating antigen immune complexes. However, the role of the C3 complement system remains largely unknown in influenza virus M2 extracellular (M2e) domain or hemagglutinin (HA) vaccine-mediated protection after vaccination. Using a C3 knockout (C3 KO) mouse model, we found that complement protein C3 was required for effective induction of immune responses to vaccination with M2e-based or HA-based vaccines, which include isotype class-switched antibodies and effector CD4 and CD8 T cell responses. C3 KO mice after active immunization with cross protective non-neutralizing M2e-based vaccine were not protected against influenza virus although low levels of M2e specific antibodies were protective after passive co-administration with virus in wild type mice. In contrast, C3 KO mice that were immunized with strain-specific neutralizing HA-based vaccine were protected against homologous virus challenge despite lower levels of HA antibody responses. C3 KO mice showed impaired maintenance of innate immune cells and a defect in innate immune responses upon exposure to antigens. The findings in this study suggest that C3 is required for effective induction of humoral and cellular adaptive immune responses as well as protective immunity after non-neutralizing influenza M2e vaccination.IMPORTANCEComplement is the well-known innate immune defense system by involving in the opsonization and lysis of pathogens but less studied in establishing adaptive immunity after vaccination. Influenza virus HA-based vaccination confers protection via strain-specific neutralizing antibodies whereas M2e-based vaccination induces a broad spectrum of protection by immunity against the conserved M2e epitopes. This study revealed the critical roles of C3 complement in inducing humoral and cellular immune responses after immunization with M2e or HA vaccines. C3 was found to be required for protection by M2e-based but not by HA-based active vaccination as well as for maintaining innate antigen presenting cells. Findings in this study have insight into better understanding the roles of C3 complement in inducing effective innate and adaptive immunity as well as in conferring protection by cross protective conserved M2e vaccination.
PMID: 30068650 DOI: 10.1128/JVI.00969-18