Immunological evidence of an early seroconversion to oncogenic Merkel cell polyomavirus in healthy children and young adults. Issue 4 (11th December 2022)
- Record Type:
- Journal Article
- Title:
- Immunological evidence of an early seroconversion to oncogenic Merkel cell polyomavirus in healthy children and young adults. Issue 4 (11th December 2022)
- Main Title:
- Immunological evidence of an early seroconversion to oncogenic Merkel cell polyomavirus in healthy children and young adults
- Authors:
- Mazziotta, Chiara
Lanzillotti, Carmen
Govoni, Marcello
Falzoni, Simonetta
Tramarin, Maria Letizia
Mazzoni, Elisa
Tognon, Mauro
Martini, Fernanda
Rotondo, John Charles - Abstract:
- Abstract: Oncogenic Merkel cell polyomavirus (MCPyV) provokes a widespread and asymptomatic infection in humans. Herein, sera from healthy children and young adults (HC, n = 344) aged 0–20 years old were evaluated for anti‐MCPyV immunoglobulin G (IgG) and IgM antibodies employing a recently developed immunoassay. Serum MCPyV IgG data from healthy subjects (HS, n = 510) and elderlies (ES, n = 226), aged 21–65/66–100 years old, from our previous studies, were included. The anti‐MCPyV IgG and IgM rates in HC sera were 40.7% and 29.7%, respectively. A lower prevalence of anti‐MCPyV IgGs was found in HC aged 0–5 years old (13%) compared to 6–10 (52.3%), 11–15 (60.5%) and 16–20 years old (61.6%) cohorts. Age‐stratified HCs exhibited similar anti‐MCPyV IgM rates (27.9%–32.9%). Serological profiles indicated that anti‐MCPyV IgGs and IgMs had low optical densities (ODs) during the first years of life, while IgM ODs appeared to decrease throughout young adulthood. A lower anti‐MCPyV IgGs rate was found in HC (40.7%) than HS (61.8%) and ES (63.7%). Upon the 5‐years range age‐stratification, a lower anti‐MCPyV IgGs rate was found in the younger HC cohort aged 0–5 years old compared to the remaining older HC/HS/ES cohorts (52.3%–72%). The younger HC cohort exhibited the lowest anti‐MCPyV IgG ODs than the older cohorts. Low anti‐MCPyV IgMs rates and ODs were found in the 21–25 (17.5%) and 26–30 (7.7%) years old cohorts. Our data indicate that, upon an early‐in‐life seroconversion, theAbstract: Oncogenic Merkel cell polyomavirus (MCPyV) provokes a widespread and asymptomatic infection in humans. Herein, sera from healthy children and young adults (HC, n = 344) aged 0–20 years old were evaluated for anti‐MCPyV immunoglobulin G (IgG) and IgM antibodies employing a recently developed immunoassay. Serum MCPyV IgG data from healthy subjects (HS, n = 510) and elderlies (ES, n = 226), aged 21–65/66–100 years old, from our previous studies, were included. The anti‐MCPyV IgG and IgM rates in HC sera were 40.7% and 29.7%, respectively. A lower prevalence of anti‐MCPyV IgGs was found in HC aged 0–5 years old (13%) compared to 6–10 (52.3%), 11–15 (60.5%) and 16–20 years old (61.6%) cohorts. Age‐stratified HCs exhibited similar anti‐MCPyV IgM rates (27.9%–32.9%). Serological profiles indicated that anti‐MCPyV IgGs and IgMs had low optical densities (ODs) during the first years of life, while IgM ODs appeared to decrease throughout young adulthood. A lower anti‐MCPyV IgGs rate was found in HC (40.7%) than HS (61.8%) and ES (63.7%). Upon the 5‐years range age‐stratification, a lower anti‐MCPyV IgGs rate was found in the younger HC cohort aged 0–5 years old compared to the remaining older HC/HS/ES cohorts (52.3%–72%). The younger HC cohort exhibited the lowest anti‐MCPyV IgG ODs than the older cohorts. Low anti‐MCPyV IgMs rates and ODs were found in the 21–25 (17.5%) and 26–30 (7.7%) years old cohorts. Our data indicate that, upon an early‐in‐life seroconversion, the seropositivity for oncogenic MCPyV peaks in late childhood/young adulthood and remains at high prevalence and relatively stable throughout life. Abstract : Herein, sera from healthy children and young adults (HC, n = 344) aged 0–20 years old were evaluated for anti‐Merkel cell polyomavirus (MCPyV) immunoglobulin G (IgG) and IgM antibodies employing a recently developed immunoassay, while MCPyV IgG data from healthy subjects (HS, n = 548) and elderlies (ES, n = 226), aged 21–65/66–100 years old, from our previous studies, were included. Our data indicate that, upon an early‐in‐life seroconversion, the seropositivity for oncogenic MCPyV peaks in late childhood/young adulthood and remains at high prevalence and relatively stable throughout life. … (more)
- Is Part Of:
- Immunology. Volume 168:Issue 4(2023)
- Journal:
- Immunology
- Issue:
- Volume 168:Issue 4(2023)
- Issue Display:
- Volume 168, Issue 4 (2023)
- Year:
- 2023
- Volume:
- 168
- Issue:
- 4
- Issue Sort Value:
- 2023-0168-0004-0000
- Page Start:
- 671
- Page End:
- 683
- Publication Date:
- 2022-12-11
- Subjects:
- adults -- antibodies -- children -- elderly -- enzyme‐linked immunosorbent assay -- immune system -- immunological assay -- MCPyV -- Merkel cell carcinoma -- Merkel cell polyomavirus -- young adults
Immunology -- Periodicals - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2567 ↗
http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=imm&close=1997#C1997 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/imm.13601 ↗
- Languages:
- English
- ISSNs:
- 0019-2805
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- Legaldeposit
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