Lokesh Sharma

Dr. Lokesh Sharma

Section of Pulmonary and Critical Care and Sleep Medicine, Yale University School of Medicine, New Haven, CT 06520, USA
orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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21 August 2019 in Nature
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Journal Article
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ASAngel G. Solis
Angel G. Solis
PBPiotr Bielecki
Piotr Bielecki
HSHolly R. Steach
Holly R. Steach
LSLokesh Sharma
Lokesh Sharma
CHChristian C. D. Harman
Christian C. D. Harman
RFRichard A. Flavell
Richard A. Flavell

22 December 2021 in Frontiers in Microbiology
Verified
Journal Article
Open access
DCDe Chang
De Chang
LSLokesh Sharma
Lokesh Sharma
CCCharles S. Dela Cruz
Charles S. Dela Cruz
DZDong Zhang
Dong Zhang
Klebsiella species cause infections at multiple sites, including lung, urinary tract, bloodstream, wound or surgical site, and brain. These infections are more likely to occur in people with preexisting health conditions. Klebsiella pneumoniae (K. pneumoniae) has emerged as a major pathogen of international concern due to the increasing incidences of hypervirulent and carbapenem-resistant strains. It is imperative to understand risk factors, prevention strategies, and therapeutic avenues to treat multidrug-resistant Klebsiella infections. Here, we highlight the epidemiology, risk factors, and control strategies against K. pneumoniae infections to highlight the grave risk posed by this pathogen and currently available options to treat Klebsiella-associated diseases.

1 March 2017 in Clinical Reviews in Allergy & Immunology
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Journal Article
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DKDaniel Elieh Ali Komi
Daniel Elieh Ali Komi
LSLokesh Sharma
Lokesh Sharma
CCCharles S. Dela Cruz
Charles S. Dela Cruz

21 January 2022 in Nature Communications
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Journal Article
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AUAvraham Unterman
Avraham Unterman
TSTomokazu S. Sumida
Tomokazu S. Sumida
NNNIMA NOURI
NIMA NOURI
XYXiting Yan
Xiting Yan
AZAmy Y. Zhao
Amy Y. Zhao
CCCharles S. Dela Cruz
Charles S. Dela Cruz
Dysregulated immune responses against the SARS-CoV-2 virus are instrumental in severe COVID-19. However, the immune signatures associated with immunopathology are poorly understood. Here we use multi-omics single-cell analysis to probe the dynamic immune responses in hospitalized patients with stable or progressive course of COVID-19, explore V(D)J repertoires, and assess the cellular effects of tocilizumab. Coordinated profiling of gene expression and cell lineage protein markers shows that S100Ahi/HLA-DRlo classical monocytes and activated LAG-3hi T cells are hallmarks of progressive disease and highlights the abnormal MHC-II/LAG-3 interaction on myeloid and T cells, respectively. We also find skewed T cell receptor repertories in expanded effector CD8+ clones, unmutated IGHG+ B cell clones, and mutated B cell clones with stable somatic hypermutation frequency over time. In conclusion, our in-depth immune profiling reveals dyssynchrony of the innate and adaptive immune interaction in progressive COVID-19.

22 July 2019 in Thorax
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Journal Article
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DUO ZHANGDUO ZHANG
DUO ZHANG
HLHeedoo Lee
Heedoo Lee
XWXiaoyun Wang
Xiaoyun Wang
MGMichael Groot
Michael Groot
LSLokesh Sharma
Lokesh Sharma
YJYang Jin
Yang Jin
Background: Uncontrolled lung inflammation is one of the prominent features in the pathogenesis of lung infection- associated acute lung injury (ALI). Microvesicles (MVs) are extracellular nanovesicles that are generated via direct membrane budding.Methods: Bronchoalveolar lavage fluid (BALF) samples were collected from mice with or without intratracheal lipopolysaccharide (LPS) instillation. BALF MVs were characterised and MV-containing microRNA (miRNA) profiles were assessed and confirmed. Secretion and function of MV-containing miR-223/142 (MV-miR-223/142) were analysed in vivo.Results: In BALF, MVs are mainly derived from macrophages in response to LPS. After intratracheal instillation (i.t.) of LPS orKlebsiella pneumoniae, MV-containing miR-223/142 are dramatically induced in both BALF and serum. Mechanistically, miRNA 3′ end uridylation mediates the packing of miR-223/142 into MVs. To investigate the functional role of MV-miR-223/142, we loaded miR-223/142 mimics into unstimulated MVs and delivered them into the murine lungs via i.t. The miR-223/142 mimics-enriched MVs selectively targeted lung macrophages and suppressed the inflammatory lung responses that were triggered by LPS orK. pneumoniae. Mechanistically, miR-223 and miR-142 synergistically suppress Nlrp3 inflammasome activation in macrophages via inhibition of Nlrp3 and Asc, respectively.Conclusions: In the pathogenesis of lung macrophage-mediated inflammatory responses, MV-miR-223/142 secretion is robustly enhanced and detectable in BALF and serum. Furthermore, restoration of intracellular miR-223/142 via vesicle-mediated delivery suppresses macrophage activation and lung inflammation via inhibition of Nlrp3 inflammasome activation.

15 September 2016 in Nature Communications
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Journal Article
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CLChang-Min Lee
Chang-Min Lee
CHChuan Hua He
Chuan Hua He
ANAdel M. Nour
Adel M. Nour
YZYang Zhou
Yang Zhou
BMBing Ma
Bing Ma
JEJack A. Elias
Jack A. Elias
Recent studies demonstrated that chitinase 3-like-1 (Chi3l1) binds to and signals via IL-13Rα2. However, the mechanism that IL-13Rα2 uses to mediate the effects of Chi3l1 has not been defined. Here, we demonstrate that the membrane protein, TMEM219, is a binding partner of IL-13Rα2 using yeast two-hybrid, co-immunoprecipitation, co-localization and bimolecular fluorescence complementation assays. Furthermore, fluorescence anisotropy nanodisc assays revealed a direct physical interaction between TMEM219 and IL-13Rα2-Chi3l1 complexes. Null mutations or siRNA silencing of TMEM219 or IL-13Rα2 similarly decreased Chi3l1-stimulated epithelial cell HB-EGF production and macrophage MAPK/Erk and PKB/Akt activation. Null mutations of TMEM219 or IL-13Rα2 also phenocopied one another as regards the ability of Chi3l1 to inhibit oxidant-induced apoptosis and lung injury, promote melanoma metastasis and stimulate TGF-β1. TMEM219 also contributed to the decoy function of IL-13Rα2. These studies demonstrate that TMEM219 plays a critical role in Chi3l1-induced IL-13Rα2 mediated signalling and tissue responses.