Monoclonal antibodies from humans with Mycobacterium tuberculosis exposure or latent infection recognize distinct arabinomannan epitopes
© 2021. The Author(s)..
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.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2021 |
---|---|
Erschienen: |
2021 |
Enthalten in: |
Zur Gesamtaufnahme - volume:4 |
---|---|
Enthalten in: |
Communications biology - 4(2021), 1 vom: 12. Okt., Seite 1181 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Ishida, Elise [VerfasserIn] |
---|
Links: |
---|
Themen: |
Antibodies, Bacterial |
---|
Anmerkungen: |
Date Completed 22.12.2021 Date Revised 22.12.2021 published: Electronic Dryad: 10.5061/dryad.dv41ns200 Citation Status MEDLINE |
---|
doi: |
10.1038/s42003-021-02714-w |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM331832445 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM331832445 | ||
003 | DE-627 | ||
005 | 20231225214335.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2021 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1038/s42003-021-02714-w |2 doi | |
028 | 5 | 2 | |a pubmed24n1106.xml |
035 | |a (DE-627)NLM331832445 | ||
035 | |a (NLM)34642445 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Ishida, Elise |e verfasserin |4 aut | |
245 | 1 | 0 | |a Monoclonal antibodies from humans with Mycobacterium tuberculosis exposure or latent infection recognize distinct arabinomannan epitopes |
264 | 1 | |c 2021 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 22.12.2021 | ||
500 | |a Date Revised 22.12.2021 | ||
500 | |a published: Electronic | ||
500 | |a Dryad: 10.5061/dryad.dv41ns200 | ||
500 | |a Citation Status MEDLINE | ||
520 | |a © 2021. The Author(s). | ||
520 | |a 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 | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, N.I.H., Extramural | |
650 | 7 | |a Antibodies, Bacterial |2 NLM | |
650 | 7 | |a Antibodies, Monoclonal |2 NLM | |
700 | 1 | |a Corrigan, Devin T |e verfasserin |4 aut | |
700 | 1 | |a Malonis, Ryan J |e verfasserin |4 aut | |
700 | 1 | |a Hofmann, Daniel |e verfasserin |4 aut | |
700 | 1 | |a Chen, Tingting |e verfasserin |4 aut | |
700 | 1 | |a Amin, Anita G |e verfasserin |4 aut | |
700 | 1 | |a Chatterjee, Delphi |e verfasserin |4 aut | |
700 | 1 | |a Joe, Maju |e verfasserin |4 aut | |
700 | 1 | |a Lowary, Todd L |e verfasserin |4 aut | |
700 | 1 | |a Lai, Jonathan R |e verfasserin |4 aut | |
700 | 1 | |a Achkar, Jacqueline M |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Communications biology |d 2018 |g 4(2021), 1 vom: 12. Okt., Seite 1181 |w (DE-627)NLM284287245 |x 2399-3642 |7 nnns |
773 | 1 | 8 | |g volume:4 |g year:2021 |g number:1 |g day:12 |g month:10 |g pages:1181 |
856 | 4 | 0 | |u http://dx.doi.org/10.1038/s42003-021-02714-w |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 4 |j 2021 |e 1 |b 12 |c 10 |h 1181 |