Seroprevalence of COVID-19 of cancer patients in Tanzania

  • Funded by National Institutes of Health (NIH)
  • Total publications:0 publications

Grant number: 3U54CA190155-05S2

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2020
    2021
  • Known Financial Commitments (USD)

    $147,415
  • Funder

    National Institutes of Health (NIH)
  • Principal Investigator

    Charles Wood
  • Research Location

    Tanzania, United States of America
  • Lead Research Institution

    University Of Nebraska Lincoln
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Immunity

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Unspecified

  • Vulnerable Population

    Other

  • Occupations of Interest

    Unspecified

Abstract

The SARS-coronavirus-2 (SARS-CoV-2) has rapidly spread worldwide causing the global pandemic. There are a number of comorbidities and risk factors associated with COVID-19 and cancer patients could be at particular higher risk since they tend to be older, likely to have multiple comorbidities, and are often immunosuppressed due to the disease and cancer treatment. Our team has been collaborating with the Ocean Road Cancer Institute (ORCI) in Dar es Salaam, Tanzania through an NCI U54 CA190155 Cancer Research International Training and Intervention Consortium project to study HIV/AIDS associated cancers in Tanzania. As part of that collaboration, we investigated the prevalence of a number of other common infectious agents in the population, such as the Kaposi's sarcoma herpesvirus, hepatitis and HIV, by testing plasma collected from cancer patients and blood bank donors. Because this collection was prior to the COVID-19 pandemic, we have retested some of them recently and have detected antibody responses that appear to target the SARS-CoV-2 proteins. This suggests that cross-reactive antibodies were present in a portion of the Tanzanian population prior to the outbreak, which could confer some protection against SARS-CoV-2. Thus, our overall objective is to develop a better understanding of potential immunological factors that may contribute to partial protection against SARS-CoV-2 infection and COVID-19 disease pathogenesis in cancer patients in Tanzania. We hypothesize that cross- reactive antibodies against different strains of coronaviruses in Africa are present prior to the pandemic, which will provide cross protection to prevent an increase of SARS-CoV-2 infection and COVID-19, in both cancer patients and the general population in Tanzania during the pandemic. Our specific aim is to determine and compare the prevalence of anti-SARS-CoV-2 antibodies among cancer patients and the general population, prior to and during the current COVID-19 pandemic. This will be carried out by: a) analyzing the cancer patients plasma collected by our ongoing U54 current prior to the pandemic and those collected from a prospective cohort of cancer patients recruited during the pandemic by this proposed study, for the presence of anti-SARS-CoV-2 antibodies; b) analyzing a large panel of normal blood donors collected prior to the pandemic and a second panel collected prospectively by this study during the current pandemic; c) compare the prevalence of anti-SARS-CoV-2 antibodies between cancer patients and the general population before and during the current pandemic. The proposed study is significant and timely because it will synergize with our ongoing U54 project and utilize its collected patients' specimen, to determine the protective effect of cross-reactive antibodies to SARS-CoV-2 in both HIV-1 infected and uninfected cancer patients in comparison to the general population, both prior to and during the current pandemic.