Influenza A virus (IAV) infections have claimed over 50 million lives worldwide during epidemic and pandemics. Patients with asthma were less likely to suffer from severe influenza during the 2009 influenza pandemic compared to non-asthmatics for reasons not yet fully elucidated. We have recapitulated these clinical findings using our innovative mouse model of asthma and influenza co-morbidity, and found that heightened eosinophilia during influenza infection correlated with reduced lung viral burden. Our preliminary data showed that eosinophil transfer into lungs of virus-infected animals reduced lung viral burden and led to increased recruitment of CD8+ T-cells into the airways. Mice in the asthma and influenza co-morbidity model also have elevated gene expression of resistin-like molecule (RELM)-? and -?, and the administration of these proteins into the lungs of virus-infected mice led to a reduction in lung viral burden and increased recruitment of CD8+ T-cells. These data led to our central hypothesis that eosinophils in allergic airways promote antiviral immunity against IAV by activating CD8+ T-cells. The three overlapping aims to be investigated in this project are: (1) To identify eosinophil granule proteins released during degranulation upon direct contact with IAV and determine their impact on IAV infectivity, (2) To determine if eosinophils directly enhance CD8+ T-cell responses against IAV, and (3) To determine the function of eosinophil-derived RELM proteins in enhancing antiviral immunity against IAV. This project is significant because we propose to identify basic immune mechanisms in host defense against a prominent human pathogen with an innovative approach of investigating eosinophils as a regulator of adaptive immunity and mediator of host protection rather than as an end-stage effector cell. These studies will have a broad impact on eosinophil biology, virology, and may offer novel therapeutic targets to treat influenza.

Public Health Relevance

We propose studies to investigate the mechanisms by which eosinophils regulate antiviral host immunity against influenza A virus. These studies are relevant to public health because they will provide mechanistic insight into anti-influenza immunity in hosts with allergic asthma. Evidence of cytotoxic T-cell regulation by eosinophils will be broadly applicable to immunology and other diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI125481-05
Application #
10102168
Study Section
Immunity and Host Defense (IHD)
Program Officer
Lane, Mary Chelsea
Project Start
2017-03-06
Project End
2022-02-28
Budget Start
2021-03-01
Budget End
2022-02-28
Support Year
5
Fiscal Year
2021
Total Cost
Indirect Cost
Name
University of Tennessee Health Science Center
Department
Pediatrics
Type
Schools of Medicine
DUNS #
941884009
City
Memphis
State
TN
Country
United States
Zip Code
38103
Veerapandian, Raja; Snyder, John D; Samarasinghe, Amali E (2018) Influenza in Asthmatics: For Better or for Worse? Front Immunol 9:1843
Lew, D Betty; LeMessurier, Kim S; Palipane, Maneesha et al. (2018) Saccharomyces cerevisiae-Derived Mannan Does Not Alter Immune Responses to Aspergillus Allergens. Biomed Res Int 2018:3298378
Doorley, Laura A; LeMessurier, Kim S; Iverson, Amy R et al. (2017) Humoral immune responses during asthma and influenza co-morbidity in mice. Immunobiology 222:1064-1073