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Monoclonal antibodies from humans with Mycobacterium tuberculosis exposure or latent infection recognize distinct arabinomannan epitopes.
Ishida, Elise; Corrigan, Devin T; Malonis, Ryan J; Hofmann, Daniel; Chen, Tingting; Amin, Anita G; Chatterjee, Delphi; Joe, Maju; Lowary, Todd L; Lai, Jonathan R; Achkar, Jacqueline M.
Affiliation
  • Ishida E; Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Corrigan DT; Department of Medicine, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Malonis RJ; Department of Biochemistry, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Hofmann D; Department of Biochemistry, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Chen T; Department of Medicine, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Amin AG; Mycobacteria Research Laboratories, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, USA.
  • Chatterjee D; Mycobacteria Research Laboratories, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, USA.
  • Joe M; Department of Chemistry, University of Alberta, Edmonton, AB, Canada.
  • Lowary TL; Department of Chemistry, University of Alberta, Edmonton, AB, Canada.
  • Lai JR; Institute of Biological Chemistry, Academia Sinica, Nangang, Taipei, Taiwan.
  • Achkar JM; Institute of Biochemical Sciences, National Taiwan University, Taipei, Taiwan.
Commun Biol ; 4(1): 1181, 2021 10 12.
Article in En | MEDLINE | ID: mdl-34642445
ABSTRACT
The surface polysacharide arabinomannan (AM) and related glycolipid lipoarabinomannan (LAM) play critical roles in tuberculosis pathogenesis. Human antibody responses to AM/LAM are heterogenous and knowledge of reactivity to specific glycan epitopes at the monoclonal level is limited, especially in individuals who can control M. tuberculosis infection. We generated human IgG mAbs to AM/LAM from B cells of two asymptomatic individuals exposed to or latently infected with M. tuberculosis. Here, we show that two of these mAbs have high affinity to AM/LAM, are non-competing, and recognize different glycan epitopes distinct from other anti-AM/LAM mAbs reported. Both mAbs recognize virulent M. tuberculosis and nontuberculous mycobacteria with marked differences, can be used for the detection of urinary LAM, and can detect M. tuberculosis and LAM in infected lungs. These mAbs enhance our understanding of the spectrum of antibodies to AM/LAM epitopes in humans and are valuable for tuberculosis diagnostic and research applications.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tuberculosis / Latent Infection / Antibodies, Bacterial / Antibodies, Monoclonal / Mycobacterium tuberculosis Limits: Humans Language: En Journal: Commun Biol Year: 2021 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tuberculosis / Latent Infection / Antibodies, Bacterial / Antibodies, Monoclonal / Mycobacterium tuberculosis Limits: Humans Language: En Journal: Commun Biol Year: 2021 Type: Article Affiliation country: United States