Publications by authors named "Tangsathapornpong A"

Article Synopsis
  • The study aimed to evaluate a new low-cost pertussis booster vaccine with reduced doses of key components, comparing it to existing Tdap vaccines, due to a recent increase in pertussis cases.
  • Conducted in Thailand with 450 adolescents, the trial tested seroconversion rates among three vaccine groups to determine if the new vaccine was non-inferior compared to traditional options.
  • Results showed that the new vaccine (ap) had a 71% seroconversion rate for anti-FHA IgG, while Tdap had a higher rate of 94%, suggesting that the new vaccine still needs further investigation to improve immunogenicity.
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Article Synopsis
  • Respiratory syncytial virus (RSV) is a major cause of lower respiratory tract infections in young children, with many experiencing infections by age two and recurring instances later in life.
  • A study analyzed medical records of children under five diagnosed with RSV-LRTI from 2016 to 2020, finding 40.16% experienced severe cases requiring extended hospital stays or intensive care.
  • Key risk factors for severe RSV-LRTI included age under three months, existing cardiovascular, gastrointestinal, genetic, and pulmonary diseases, as well as multiple co-morbidities, resulting in significantly higher hospitalization costs and fatalities.
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Article Synopsis
  • Limited evidence exists about how much wheezing in young children is linked to respiratory syncytial virus (RSV) infections in their early years.
  • A study tracked 2-year-olds in 8 countries until they turned six, assessing wheeze occurrences and calculating the population attributable risk (PAR) for those with previous RSV lower respiratory tract infections.
  • Results showed that children with RSV-LRTI had significantly higher incidences of wheezing, suggesting that preventing RSV infections in early childhood could reduce wheezing episodes in later years.
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Article Synopsis
  • The study aimed to compare immune responses between children with hybrid immunity (from COVID-19 infection and mRNA vaccination) and those with only two vaccine doses.
  • The analysis involved 179 children with hybrid immunity and 134 with two doses, assessing their protective immune response against the Omicron strain via a surrogate virus neutralization test.
  • Results showed that children who had natural infection combined with vaccination (Groups 1 and 3) had significantly higher protective immune responses compared to those with just two vaccine doses (Group 2).
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Introduction: The number of pediatric COVID-19 infections is increasing; however, the data on long COVID conditions in children is still limited. Our study aimed to find the prevalence of long COVID in children during the Delta and Omicron waves, as well as associated factors.

Methods: A single-center prospective cohort study was conducted.

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Background And Objectives: The study of prevalence, risk factors, and vaccine effectiveness (VE) in children, adolescents, and young adults during the Omicron era has been limited, making this the objectives of the study.

Methods: A prospective, test-negative case-control study was conducted on patients aged 0-24 years old classified as patients under investigation (PUI) from January to May 2022. PUI with positive RT-PCR within 14 days were classified as cases, whilst PUI with negative RT-PCR in 14 days were controls.

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Background: Various case definitions of respiratory syncytial virus lower respiratory tract infection (RSV-LRTI) are currently proposed. We assessed the performance of 3 clinical case definitions against the World Health Organization definition recommended in 2015 (WHO 2015).

Methods: In this prospective cohort study conducted in 8 countries, 2401 children were followed up for 2 years from birth.

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The changes in the severe acute respiratory syndrome coronavirus 2 and the tapering of immunity after vaccination have propelled the need for a booster dose vaccine. We aim to evaluate B and T cell immunogenicity and reactogenicity of mRNA-1273 COVID-19 vaccine (100 µg) as a third booster dose after receiving either two doses of inactivated COVID-19 vaccine (CoronaVac) or two doses of viral vector vaccine (AZD1222) in adults not previously infected with COVID-19. The anti-receptor-binding-domain IgG (anti-RBD IgG), surrogate virus neutralization test (sVNT) against the Delta variant, and Interferon-Gamma (IFN-γ) level were measured at baseline, day (D)14 and D90 after vaccination.

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The increasing in dengue cases nowadays is a global threat concern. Fifty per cent of the world's population is vulnerable to dengue infection with Asia contributing over two-thirds of the global burden. The double trouble of Coronavirus disease 2019 (COVID-19) arising from novel severe respiratory syndrome coronavirus (SARS-CoV-2) and dengue virus is a major challenge, particularly in developing countries due to overburdened public health systems and economic constraints including the ability to diagnose.

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Objectives: To evaluate the immunogenicity of an extended interval regimen of BNT162b2 among healthy school-age children.

Methods: A randomized-control trial conducted among healthy Thai children aged 5-11 years. Participants received two doses of BNT162b2 with an 8-week (extended dosing) vs 3-week interval.

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The surge in coronavirus disease 2019 (COVID-19) caused by the Omicron variants of the severe acute respiratory syndrome coronavirus 2 necessitates researches to inform vaccine effectiveness (VE) and other preventive measures to halt the pandemic. A test-negative case-control study was conducted among adults (age ≥18 years) who were at-risk for COVID-19 and presented for nasopharyngeal real-time polymerase chain reaction testing during the Omicron variant-dominant period in Thailand (1 January 2022-15 June 2022). All participants were prospectively followed up for COVID-19 development for 14 days after the enrolment.

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Background: A primary series of 2-dose SARS-CoV-2 vaccines based on an ancestral strain generate inadequate neutralizing antibodies against the SARS-CoV-2 Omicron variant. This study aimed to describe the immune response from giving healthy school-aged children who previously received 2 inactivated vaccines an mRNA BNT162b2 booster.

Methods: Healthy children aged 5-11 years who received 2 doses of CoronaVac or Covilo were enrolled and received 10 µg BNT162b2 intramuscularly.

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Background: Due to the possibility of asymptomatic pneumonia in children with COVID-19 leading to overexposure to radiation and problems in limited-resource settings, we conducted a nationwide, multi-center study to determine the risk factors of pneumonia in children with COVID-19 in order to create a pediatric pneumonia predictive score, with score validation.

Methods: This was a retrospective cohort study done by chart review of all children aged 0-15 years admitted to 13 medical centers across Thailand during the study period. Univariate and multivariate analyses as well as backward and forward stepwise logistic regression were used to generate a final prediction model of the pneumonia score.

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To achieve the goal of measles elimination, herd immunity with 95% seroprotection in the community is required. This study aimed to describe the measles seropositivity rate among Thai children and adolescents. A cross-sectional study was conducted among children aged 3−18 years in Bangkok and its suburbs.

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Adolescents with underlying diseases are at risk of severe COVID-19. The immune response of BNT162b2 may be poor among immunocompromised adolescents. We aim to describe immunogenicity of mRNA BNT162b2 among adolescents who are immunocompromised or have chronic diseases.

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Background: The true burden of lower respiratory tract infections (LRTIs) due to respiratory syncytial virus (RSV) remains unclear. This study aimed to provide more robust, multinational data on RSV-LRTI incidence and burden in the first 2 years of life.

Methods: This prospective, observational cohort study was conducted in Argentina, Bangladesh, Canada, Finland, Honduras, South Africa, Thailand, and United States.

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Background: Few studies had focused on the epidemiological and clinical characteristics of pediatric COVID-19 (SARS-CoV-2) during Delta and pre-Delta eras in Asia, despite it being a pandemic.

Objective: To study the epidemiological and clinical characteristics of three waves of pediatric COVID-19 infections in a tertiary-care setting in Thailand.

Methods: This retrospective study reviewed all PCR-confirmed pediatric (0-18 years of age) COVID-19 infections between January 13, 2020, and October 31, 2021, in a tertiary care system in Thailand.

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Background: There were limited epidemiological data of pediatric COVID-19 in Asia outside China, especially during the era of the variants of concern such as the Delta and Alpha variants. The objective was to describe the clinical epidemiology of pediatric COVID-19 in a tertiary care center in Thailand from April to August 2021. The identification of risk factors for the development of pneumonia in these children was also performed.

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Background: Immunogenicity of inactivated SARS-CoV-2 vaccine has waning antibody over time. With the emergence of the SARS-CoV-2 delta variant, which requires higher neutralizing antibody to prevent infection, a booster dose is needed.

Objective: To evaluate immunogenicity and reactogenicity of standard- versus low-dose ChAdOx1 nCoV-19 vaccine booster after CoronaVac in healthy adults.

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Thailand has implemented single-dose mumps-containing vaccines since 1997 and two doses since 2010. This study aimed to describe the seroprevalence of mumps among children who received one- or two-dose mumps vaccines. A cross-sectional study of 145 children (aged 3-9 years) and 422 adolescents (10-18 years) was conducted.

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Rubella is generally a mild disease, but infection during pregnancy can cause congenital rubella syndrome. Thailand has implemented a two-dose MMR vaccination policy since 2010. This study aimed to describe the seroprevalence rate of rubella among children and adolescents in Thailand.

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Background: Noroviruses (NoVs) cause acute gastroenteritis (AGE) worldwide, affecting children in particular. We aimed to estimate the burden of disease due to NoV among children aged <6 years in Brazil, Chile, Philippines and Thailand.

Methods: This was a prospective, hospital-based, observational study.

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Article Synopsis
  • Immunization is the best preventive method for varicella, with Korea using the MAV/06 strain for vaccination.
  • A new vaccine, MG1111, developed using the Medical Research Council-5 cell line, was approved and its immunogenicity and safety were tested in a study with 515 children in Korea and Thailand.
  • Results showed MG1111 had a high seroconversion rate of 97.9% and comparable safety profiles to the control vaccine, Varivax, indicating it is not immunologically inferior.
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