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Genomic and Co-Evolutionary Determinants of Clinical Severity in Active Tuberculosis Patients- [electronic resource]
Genomic and Co-Evolutionary Determinants of Clinical Severity in Active Tuberculosis Patients- [electronic resource]
- 자료유형
- 학위논문
- Control Number
- 0016935486
- International Standard Book Number
- 9798380198677
- Dewey Decimal Classification Number
- 610
- Main Entry-Personal Name
- McHenry, Michael.
- Publication, Distribution, etc. (Imprint
- [S.l.] : Case Western Reserve University., 2021
- Publication, Distribution, etc. (Imprint
- Ann Arbor : ProQuest Dissertations & Theses, 2021
- Physical Description
- 1 online resource(129 p.)
- General Note
- Source: Dissertations Abstracts International, Volume: 85-03, Section: B.
- General Note
- Advisor: Bush, William.
- Dissertation Note
- Thesis (Ph.D.)--Case Western Reserve University, 2021.
- Restrictions on Access Note
- This item must not be sold to any third party vendors.
- Summary, Etc.
- 요약Tuberculosis (TB) is a major public health problem, causing more deaths globally than any other pathogen prior to COVID19. It is also the leading cause of death among people infected with human immunodeficiency virus (HIV). Susceptibility to TB can be influenced by human genetic variation. However, factors underlying variation in TB severity are less well studied. Clinical severity is an important phenotype that encompasses prognosis, patient experience, and risk of mortality. Thus, it is important to study severity, as it can help us better understand patients' quality of life, disease experience, and to predict survival among TB patients receiving treatment. There is also evidence that MTB genetic variation as delineated by phylogenetic lineage can affect TB disease severity, when considered simultaneously with human genetic variations and the interaction between the two. Many genetic studies of TB stop short of linking these genetic effects to biological function. The proposed study will address these fundamental gaps by 1) studying the genomic underpinnings of active TB severity using a meaningful, replicable, and validated clinical phenotype; 2) demonstrating evidence of co-evolution between humans and MTB on a population level how it affects severity; and 3) bridging the gap between genetic variants and immunological function by studying gene expression in the macrophage response. The overall goal is to examine how genomic variation in humans and MTB impact the immunological response to active TB disease and how this correlates with clinical severity.
- Subject Added Entry-Topical Term
- Medicine.
- Subject Added Entry-Topical Term
- Epidemiology.
- Subject Added Entry-Topical Term
- Genetics.
- Subject Added Entry-Topical Term
- Public health.
- Index Term-Uncontrolled
- Tuberculosis
- Index Term-Uncontrolled
- Genetic epidemiology
- Index Term-Uncontrolled
- Infectious disease
- Index Term-Uncontrolled
- Evolution
- Index Term-Uncontrolled
- Immunological function
- Added Entry-Corporate Name
- Case Western Reserve University Epidemiology and Biostatistics
- Host Item Entry
- Dissertations Abstracts International. 85-03B.
- Host Item Entry
- Dissertation Abstract International
- Electronic Location and Access
- 로그인을 한후 보실 수 있는 자료입니다.
- Control Number
- joongbu:642911
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