In vivo targeting of protein antigens to dendritic cells using anti‐DEC‐205 single chain antibody improves HIV Gag specific CD4+ T cell responses protecting from airway challenge with recombinant vaccinia‐gag virus. Issue 2 (13th March 2017)
- Record Type:
- Journal Article
- Title:
- In vivo targeting of protein antigens to dendritic cells using anti‐DEC‐205 single chain antibody improves HIV Gag specific CD4+ T cell responses protecting from airway challenge with recombinant vaccinia‐gag virus. Issue 2 (13th March 2017)
- Main Title:
- In vivo targeting of protein antigens to dendritic cells using anti‐DEC‐205 single chain antibody improves HIV Gag specific CD4+ T cell responses protecting from airway challenge with recombinant vaccinia‐gag virus
- Authors:
- Ngu, Loveline N.
Nji, Nadesh N.
Ambada, Georgia E.
Sagnia, Bertrand
Sake, Carol Ngane
Tchadji, Jules Colinc
Njambe Priso, Ghislain Donald
Lissom, Abel
Tchouangueu, Thibau Flaurant
Manga Tebit, Denis
Waffo, Alain Bopda
Park, Chae Gyu
Steinman, Ralph M.
Überla, Klaus
Nchinda, Godwin W. - Abstract:
- Abstract: Introduction: Targeting antigens to dendritic cells (DCs) in vivo via a DC‐restricted endocytic receptor, DEC205, has been validated to enhance immunity in several vaccine platforms. Particularly atttractive is selected delivery of proteins to DCs in vivo because it enables proteins to be more immunogenic and provides a cheaper and effective way for repeated immunizations. Methods: In this study, we tested the efficacy of a single chain antibody to DEC205 (scDEC) to deliver protein antigens selectively to DCs in vivo and to induce protective immunity. Results: In comparison to soluble Ovalbumin (OVA) antigen, when recombinant scDEC:OVA protein was injected subcutaneously (s.c.) into mice, the OVA protein was selectively presented by DCs to both TCR transgenic CD8 + and CD4 + T cells approximately 500 and 100 times more efficient than soluble OVA, respectively, and could persist for seven days following s.c. injection of the scDEC205:OVA. Similarly selective targeting of HIV Gag P24 to DCs in vivo using scDEC‐Gag protein plus polyICLC vaccine resulted in strong, long lasting, polyfuntional CD4 + T cells in mice which were protective against airway challenge by a recombinant vaccinia‐gag virus. Conclusion: Thus targeting protein antigens to DCs using scDEC can be used either alone or in combination with other strategies for effective immunization. Abstract : Targeting protein antigen in situ to dendritic cells using single chain antibody to DEC205 enhanced antigenAbstract: Introduction: Targeting antigens to dendritic cells (DCs) in vivo via a DC‐restricted endocytic receptor, DEC205, has been validated to enhance immunity in several vaccine platforms. Particularly atttractive is selected delivery of proteins to DCs in vivo because it enables proteins to be more immunogenic and provides a cheaper and effective way for repeated immunizations. Methods: In this study, we tested the efficacy of a single chain antibody to DEC205 (scDEC) to deliver protein antigens selectively to DCs in vivo and to induce protective immunity. Results: In comparison to soluble Ovalbumin (OVA) antigen, when recombinant scDEC:OVA protein was injected subcutaneously (s.c.) into mice, the OVA protein was selectively presented by DCs to both TCR transgenic CD8 + and CD4 + T cells approximately 500 and 100 times more efficient than soluble OVA, respectively, and could persist for seven days following s.c. injection of the scDEC205:OVA. Similarly selective targeting of HIV Gag P24 to DCs in vivo using scDEC‐Gag protein plus polyICLC vaccine resulted in strong, long lasting, polyfuntional CD4 + T cells in mice which were protective against airway challenge by a recombinant vaccinia‐gag virus. Conclusion: Thus targeting protein antigens to DCs using scDEC can be used either alone or in combination with other strategies for effective immunization. Abstract : Targeting protein antigen in situ to dendritic cells using single chain antibody to DEC205 enhanced antigen uptake and presentation. combining such targeting with a TLR3 ligand polyICLC enables the induction of protective CD4 + T cells in murine airway. … (more)
- Is Part Of:
- Immunity, inflammation and disease. Volume 7:Issue 2(2019)
- Journal:
- Immunity, inflammation and disease
- Issue:
- Volume 7:Issue 2(2019)
- Issue Display:
- Volume 7, Issue 2 (2019)
- Year:
- 2019
- Volume:
- 7
- Issue:
- 2
- Issue Sort Value:
- 2019-0007-0002-0000
- Page Start:
- 55
- Page End:
- 67
- Publication Date:
- 2017-03-13
- Subjects:
- Antigens -- dendritic cells -- immunization
Immunology -- Periodicals
Immunity -- Periodicals
Inflammation -- Periodicals
616.079 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2050-4527 ↗
http://onlinelibrary.wiley.com/ ↗
http://www.wileyopenaccess.com/view/journals.html ↗ - DOI:
- 10.1002/iid3.151 ↗
- Languages:
- English
- ISSNs:
- 2050-4527
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 20494.xml