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Published on: July 10, 2017
Evaluating Johnson and Johnson COVID-19 Vaccination Outcomes in a Low-Income Hispanic Population
Christopher Lamb1, Christopher Owens2, Wendy Gamboa2
1Weatherhead School of Management, Case Western Reserve University, Cleveland, OH 44106, USA.
Insights
This study assessed the Johnson & Johnson COVID-19 vaccine
Area of Science:
- Immunology
- Vaccinology
- Public Health
Background:
- Pilot study conducted at a low-income clinic.
- Focus on assessing humoral immune response to Johnson & Johnson COVID-19 vaccine (Ad26.COV2.S).
- Aimed to evaluate COVID-19 health status in a Hispanic patient population post-vaccination.
Purpose of the Study:
- To assess the humoral immune response to the Johnson & Johnson COVID-19 vaccine.
- To understand methods for evaluating COVID-19 health status in a specific demographic.
- To explore the utility of rapid antibody tests for monitoring vaccine effectiveness.
Main Methods:
- Utilized the Clungene® SARS-CoV-2 IgG/IgM Rapid Test Cassette.
- Detected antibodies targeting the receptor-binding domain (RBD) of the spike protein.
- Antibodies against the spike protein served as a measure of humoral response.
Main Results:
- Confirmed antibody waning over time, consistent with reported vaccine efficacy.
- Identified a statistically significant relationship between immune response and demographic/health variables.
- Demonstrated the potential for antibody testing to monitor vaccine effectiveness.
Conclusions:
- COVID-19 negative patients can be monitored for vaccine success and durability.
- Low-cost antibody lateral flow devices can aid physicians in assessing patient COVID-19 health status.
- Further research is recommended to confirm the clinical utility of this monitoring approach.
Background:
A pilot study was performed at a low-income emergency care clinic to assess the humoral immune response to the Johnson & Johnson (J&J) COVID-19 vaccine (Ad26.COV2.S) to better understand how to evaluate the COVID-19 health status of its Hispanic patient population following vaccination.
Methods:
This study used the Clungene® SARS-CoV-2 IgG/IgM Rapid Test Cassette to determine the presence of binding antibodies resulting from the J&J COVID-19 vaccine. The Clungene test principle is based on the receptor-binding domain (RBD) of the spike protein. Antibodies targeting the spike protein are considered an appropriate measure of humoral response from spike-based vaccines.
Results:
The study confirmed previous research that antibodies wane over time, and results are consistent with reported vaccine efficacy. There was a statistically significant relationship between the humoral immune response and demographic and health status variables.
Conclusions:
COVID-19 negative patients can be easily and efficiently monitored to determine the success and durability of COVID-19 vaccines in low-income minority populations. The use of simple low-cost spike targeted COVID-19 antibody lateral flow devices may serve as a useful adjunct to assist community-based physicians on the COVID-19 health status of its patients. Further research is needed to confirm the utility of this approach.
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