Exploratory study of humoral and cellular immunity to 17DD Yellow Fever vaccination in children and adults residents of areas without circulation of Yellow Fever Virus. Issue 5 (31st January 2022)
- Record Type:
- Journal Article
- Title:
- Exploratory study of humoral and cellular immunity to 17DD Yellow Fever vaccination in children and adults residents of areas without circulation of Yellow Fever Virus. Issue 5 (31st January 2022)
- Main Title:
- Exploratory study of humoral and cellular immunity to 17DD Yellow Fever vaccination in children and adults residents of areas without circulation of Yellow Fever Virus
- Authors:
- Reis, Laise Rodrigues
Costa-Rocha, Ismael Artur da
Campi-Azevedo, Ana Carolina
Peruhype-Magalhães, Vanessa
Coelho-dos-Reis, Jordana Grazziela
Costa-Pereira, Christiane
Otta, Dayane Andriotti
Freire, Larissa Chaves
Lima, Sheila Maria Barbosa de
Azevedo, Adriana de Souza
Schwarcz, Waleska Dias
Ano Bom, Ana Paula Dinis
Silva, Andrea Marques Vieira da
Souza, Alessandro Fonseca de
Castro, Thalita da Matta de
Ferroco, Clara Lucy de Vasconcellos
Filippis, Ana Maria Bispo de
Nogueira, Fernanda de Bruycker
Homma, Akira
Domingues, Carla Magda
Sousa, Eduardo Sérgio Soares
Camacho, Luiz Antônio Bastos
Maia, Maria de Lourdes de Souza
Teixeira-Carvalho, Andréa
Martins-Filho, Olindo Assis - Abstract:
- Abstract: The present investigation comprised two independent observational arms to evaluate the influence of pre-existing flavivirus humoral immunity and the age-impact on 17DD-YF vaccination immunity. Flavivirus (YFV; DENV; ZIKV) serology and YF-specific cellular immunity was evaluated in 288 children/9 Mths –4 Yrs and 288 adults/18–49 Yrs residents of areas without YFV circulation. Data demonstrated that flavivirus seropositivity at baseline was higher in Adults as compared to Children (26%;87%;67% vs 6%;13%;15%, respectively). The heterologous flavivirus seropositivity (DENV; ZIKV) did not impact the YF-specific cellular immune response at baseline. However, higher levels of NCD4, EMCD8, IFN-MCD8, NCD19 and nCMCD19 were observed in subjects with pre-existing YFV seropositivity. Primary vaccination of YFV-seronegative volunteers led to higher levels of YF-neutralizing antibodies in Adults as compared to Younger Children (9 Mths –2 Yrs ). Although similar seropositivity rates observed amongst Children and Adults at D30-45, lower rates were observed in Younger Children (9 Mths –2 Yrs ) at D365 (94%;95%;100% vs 87%;96%;99%, respectively). A progressive decline in antibody levels were reported at D365, being more expressive in Children as compared to Adults. All age-subgroups exhibited at D30-45 increased levels of eEfCD4, EMCD4, IFN-MCD8 and nCMCD19 together with a decrease of eEfCD8 and CMCD8. While an increase of EMCD8 were observed in all subgroups at D30-45, a declinedAbstract: The present investigation comprised two independent observational arms to evaluate the influence of pre-existing flavivirus humoral immunity and the age-impact on 17DD-YF vaccination immunity. Flavivirus (YFV; DENV; ZIKV) serology and YF-specific cellular immunity was evaluated in 288 children/9 Mths –4 Yrs and 288 adults/18–49 Yrs residents of areas without YFV circulation. Data demonstrated that flavivirus seropositivity at baseline was higher in Adults as compared to Children (26%;87%;67% vs 6%;13%;15%, respectively). The heterologous flavivirus seropositivity (DENV; ZIKV) did not impact the YF-specific cellular immune response at baseline. However, higher levels of NCD4, EMCD8, IFN-MCD8, NCD19 and nCMCD19 were observed in subjects with pre-existing YFV seropositivity. Primary vaccination of YFV-seronegative volunteers led to higher levels of YF-neutralizing antibodies in Adults as compared to Younger Children (9 Mths –2 Yrs ). Although similar seropositivity rates observed amongst Children and Adults at D30-45, lower rates were observed in Younger Children (9 Mths –2 Yrs ) at D365 (94%;95%;100% vs 87%;96%;99%, respectively). A progressive decline in antibody levels were reported at D365, being more expressive in Children as compared to Adults. All age-subgroups exhibited at D30-45 increased levels of eEfCD4, EMCD4, IFN-MCD8 and nCMCD19 together with a decrease of eEfCD8 and CMCD8. While an increase of EMCD8 were observed in all subgroups at D30-45, a declined duration at D365 was reported only in Younger Children (9 Mths –2 Yrs ). Biomarker signatures further support that only Younger Children (9 Mths –2 Yrs ) presented a progressive decline of EMCD8 at D365. Together, these findings demonstrated that regardless the similarities observed in YF-neutralizing antibodies, the age impacts the duration of cellular immune response to primary 17DD-YF vaccination. … (more)
- Is Part Of:
- Vaccine. Volume 40:Issue 5(2022)
- Journal:
- Vaccine
- Issue:
- Volume 40:Issue 5(2022)
- Issue Display:
- Volume 40, Issue 5 (2022)
- Year:
- 2022
- Volume:
- 40
- Issue:
- 5
- Issue Sort Value:
- 2022-0040-0005-0000
- Page Start:
- 798
- Page End:
- 810
- Publication Date:
- 2022-01-31
- Subjects:
- Yellow Fever -- 17DD vaccine -- Neutralizing antibodies -- Cellular memory -- Children -- Adults
Vaccines -- Periodicals
615.372 - Journal URLs:
- http://www.sciencedirect.com/science/journal/0264410X ↗
http://www.clinicalkey.com/dura/browse/journalIssue/0264410X ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/0264410X ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.vaccine.2021.12.029 ↗
- Languages:
- English
- ISSNs:
- 0264-410X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9138.628000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 20637.xml