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Scientific reports · 2022

Humoral and cellular immune responses to Lassa fever virus in Lassa fever survivors and their exposed contacts in Southern Nigeria.

СтатьяПоддержка исследования: вне правительства СШАПоддержка NIH: внешняя программаНазвание и аннотация: Перевод в очереди
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Ugwu Chinedu, Olumade Testimony, Nwakpakpa Ebenezer, Onyia Venatius, Odeh Elizabeth, Duruiheoma Rosemary Ogonna, Ojide Chiedozie K, Eke Matthew Afam, Nwafor Ifeanyi Emmanuel, Chika-Igwenyi Nneka, Abu Augustine M, Azuogu Benedict, Ajayi Nnennaya, Ogah Emeka, Ayodeji Oluwafemi, Abejegah Chukwuyem, Adedosu Nelson, Oyejide Nicholas, Abah Sylvester, Omidele Abiola, Ingbian Winifred, Osoba Emmanuel, Eromon Philomena, Oluniyi Paul, Ogunsanya Olusola, Happi Anise, Otuh Patricia, Nadesalingam Angalee, Carnell George, Krause Nina, Aguinam Ernest, Kinsley Rebecca, Storisteanu Daniel Matthew L, Tonks Paul, Nelson Diana, McAlister Carley, Boisen Matthew, Garry Robert, Wright Edward, Temperton Nigel, Frost Simon, Heeney Jonathan Luke, Happi Christian

Аннотация

Elucidating the adaptive immune characteristics of natural protection to Lassa fever (LF) is vital in designing and selecting optimal vaccine candidates. With rejuvenated interest in LF and a call for accelerated research on the Lassa virus (LASV) vaccine, there is a need to define the correlates of natural protective immune responses to LF. Here, we describe cellular and antibody immune responses present in survivors of LF (N = 370) and their exposed contacts (N = 170) in a LASV endemic region in Nigeria. Interestingly, our data showed comparable T cell and binding antibody responses from both survivors and their contacts, while neutralizing antibody responses were primarily seen in the LF survivors and not their contacts. Neutralizing antibody responses were found to be cross-reactive against all five lineages of LASV with a strong bias to Lineage II, the prevalent strain in southern Nigeria. We demonstrated that both T cell and antibody responses were not detectable in peripheral blood after a decade in LF survivors. Notably LF survivors maintained high levels of detectable binding antibody response for six months while their contacts did not. Lastly, as potential vaccine targets, we identified the regions of the LASV Glycoprotein (GP) and Nucleoprotein (NP) that induced the broadest peptide-specific T cell responses. Taken together this data informs immunological readouts and potential benchmarks for clinical trials evaluating LASV vaccine candidates.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты