학술논문
Endothelial eNAMPT amplifies pre-clinical acute lung injury: efficacy of an eNAMPT-neutralising monoclonal antibody.
Document Type
Academic Journal
Author
Quijada H; Dept of Medicine, University of Arizona Health Sciences, Tucson, AZ, USA.; Co-first authors.; Bermudez T; Dept of Medicine, University of Arizona Health Sciences, Tucson, AZ, USA.; Co-first authors.; Kempf CL; Dept of Medicine, University of Arizona Health Sciences, Tucson, AZ, USA.; Valera DG; Dept of Medicine, University of Arizona Health Sciences, Tucson, AZ, USA.; Garcia AN; Dept of Radiation Oncology, University of Arizona Health Sciences, Tucson, AZ, USA.; Camp SM; Dept of Medicine, University of Arizona Health Sciences, Tucson, AZ, USA.; Song JH; Dept of Medicine, University of Arizona Health Sciences, Tucson, AZ, USA.; Franco E; Dept of Medicine, University of Arizona Health Sciences, Tucson, AZ, USA.; Burt JK; Dept of Medicine, University of Arizona Health Sciences, Tucson, AZ, USA.; Sun B; Dept of Pathology, University of Arizona Health Sciences, Tucson, AZ, USA.; Mascarenhas JB; Dept of Medicine, University of Arizona Health Sciences, Tucson, AZ, USA.; Burns K; Dept of Medicine, University of Arizona Health Sciences, Tucson, AZ, USA.; Gaber A; Dept of Medicine, University of Arizona Health Sciences, Tucson, AZ, USA.; Oita RC; Dept of Medicine, University of Arizona Health Sciences, Tucson, AZ, USA.; Reyes Hernon V; Dept of Medicine, University of Arizona Health Sciences, Tucson, AZ, USA.; Barber C; Dept of Medical Imaging, University of Arizona Health Sciences, Tucson, AZ, USA.; Moreno-Vinasco L; Dept of Medicine, University of Arizona Health Sciences, Tucson, AZ, USA.; Sun X; Dept of Medicine, University of Arizona Health Sciences, Tucson, AZ, USA.; Cress AE; Dept of Cellular and Molecular Medicine, University of Arizona Health Sciences, Tucson, AZ, USA.; Martin D; Houston Methodist Hospital Research Institute, Houston, TX, USA.; Liu Z; Dept of Medical Imaging, University of Arizona Health Sciences, Tucson, AZ, USA.; Desai AA; Dept of Medicine, Indiana University, Indianapolis IN, USA.; Natarajan V; Dept of Medicine, University of Illinois Chicago, Chicago, IL, USA.; Jacobson JR; Dept of Medicine, University of Illinois Chicago, Chicago, IL, USA.; Dudek SM; Dept of Medicine, University of Illinois Chicago, Chicago, IL, USA.; Bime C; Dept of Medicine, University of Arizona Health Sciences, Tucson, AZ, USA.; Sammani S; Dept of Medicine, University of Arizona Health Sciences, Tucson, AZ, USA.; Co-senior authors.; Garcia JGN; Dept of Medicine, University of Arizona Health Sciences, Tucson, AZ, USA.; Co-senior authors.
Source
Publisher: European Respiratory Society Country of Publication: England NLM ID: 8803460 Publication Model: Electronic-Print Cited Medium: Internet ISSN: 1399-3003 (Electronic) Linking ISSN: 09031936 NLM ISO Abbreviation: Eur Respir J Subsets: MEDLINE
Subject
Language
English
Abstract
Rationale: The severe acute respiratory syndrome coronavirus 2/coronavirus disease 2019 pandemic has highlighted the serious unmet need for effective therapies that reduce acute respiratory distress syndrome (ARDS) mortality. We explored whether extracellular nicotinamide phosphoribosyltransferase (eNAMPT), a ligand for Toll-like receptor (TLR)4 and a master regulator of innate immunity and inflammation, is a potential ARDS therapeutic target.
Methods: Wild-type C57BL/6J or endothelial cell (EC)-c NAMPT-/- knockout mice (targeted EC NAMPT deletion) were exposed to either a lipopolysaccharide (LPS)-induced ("one-hit") or a combined LPS/ventilator ("two-hit")-induced acute inflammatory lung injury model. A NAMPT-specific monoclonal antibody (mAb) imaging probe ( 99m Tc-ProNamptor) was used to detect NAMPT expression in lung tissues. Either an eNAMPT-neutralising goat polyclonal antibody (pAb) or a humanised monoclonal antibody (ALT-100 mAb) were used in vitro and in vivo .
Results: Immunohistochemical, biochemical and imaging studies validated time-dependent increases in NAMPT lung tissue expression in both pre-clinical ARDS models. Intravenous delivery of either eNAMPT-neutralising pAb or mAb significantly attenuated inflammatory lung injury (haematoxylin and eosin staining, bronchoalveolar lavage (BAL) protein, BAL polymorphonuclear cells, plasma interleukin-6) in both pre-clinical models. In vitro human lung EC studies demonstrated eNAMPT-neutralising antibodies (pAb, mAb) to strongly abrogate eNAMPT-induced TLR4 pathway activation and EC barrier disruption. In vivo studies in wild-type and EC-c NAMPT-/- mice confirmed a highly significant contribution of EC-derived NAMPT to the severity of inflammatory lung injury in both pre-clinical ARDS models.
Conclusions: These findings highlight both the role of EC-derived eNAMPT and the potential for biologic targeting of the eNAMPT/TLR4 inflammatory pathway. In combination with predictive eNAMPT biomarker and NAMPT genotyping assays, this offers the opportunity to identify high-risk ARDS subjects for delivery of personalised medicine.
Competing Interests: Conflict of interest: H. Quijada has nothing to disclose. Conflict of interest: T. Bermudez has nothing to disclose. Conflict of interest: C.L. Kempf has nothing to disclose. Conflict of interest: D.G. Valera has nothing to disclose. Conflict of interest: A.N. Garcia has nothing to disclose. Conflict of interest: S.M. Camp has nothing to disclose. Conflict of interest: J.H. Song has nothing to disclose. Conflict of interest: E. Franco has nothing to disclose. Conflict of interest: J.K. Burt has nothing to disclose. Conflict of interest: B. Sun has nothing to disclose. Conflict of interest: J.B. Mascarenhas has nothing to disclose. Conflict of interest: K. Burns has nothing to disclose. Conflict of interest: A. Gaber has nothing to disclose. Conflict of interest: R.C. Oita has nothing to disclose. Conflict of interest: V. Reyes Hernon has nothing to disclose. Conflict of interest: C. Barber has nothing to disclose. Conflict of interest: L. Moreno-Vinasco has nothing to disclose. Conflict of interest: X. Sun has nothing to disclose. Conflict of interest: A.E. Cress has nothing to disclose. Conflict of interest: D. Martin has investments in Aqualung, outside the submitted work. Conflict of interest: Z. Liu has nothing to disclose. Conflict of interest: A.A. Desai reports grants from NIH R01 (HL136603) and consultancy for Novartis, outside the submitted work. Conflict of interest: V. Natarajan has nothing to disclose. Conflict of interest: J.R. Jacobson has nothing to disclose. Conflict of interest: S.M. Dudek has nothing to disclose. Conflict of interest: C. Bime has nothing to disclose. Conflict of interest: S. Sammani has nothing to disclose. Conflict of interest: J.G.N. Garcia reports grants and non-financial support (provision of research materials) from Aqualung Therapeutics, Corp., during the conduct of the study; grants and personal fees from Aqualung Therapeutics, Corp., outside the submitted work; and has a US Patent No. 9,409,983 issued.
(Copyright ©ERS 2021.)
Methods: Wild-type C57BL/6J or endothelial cell (EC)-c NAMPT
Results: Immunohistochemical, biochemical and imaging studies validated time-dependent increases in NAMPT lung tissue expression in both pre-clinical ARDS models. Intravenous delivery of either eNAMPT-neutralising pAb or mAb significantly attenuated inflammatory lung injury (haematoxylin and eosin staining, bronchoalveolar lavage (BAL) protein, BAL polymorphonuclear cells, plasma interleukin-6) in both pre-clinical models. In vitro human lung EC studies demonstrated eNAMPT-neutralising antibodies (pAb, mAb) to strongly abrogate eNAMPT-induced TLR4 pathway activation and EC barrier disruption. In vivo studies in wild-type and EC-c NAMPT
Conclusions: These findings highlight both the role of EC-derived eNAMPT and the potential for biologic targeting of the eNAMPT/TLR4 inflammatory pathway. In combination with predictive eNAMPT biomarker and NAMPT genotyping assays, this offers the opportunity to identify high-risk ARDS subjects for delivery of personalised medicine.
Competing Interests: Conflict of interest: H. Quijada has nothing to disclose. Conflict of interest: T. Bermudez has nothing to disclose. Conflict of interest: C.L. Kempf has nothing to disclose. Conflict of interest: D.G. Valera has nothing to disclose. Conflict of interest: A.N. Garcia has nothing to disclose. Conflict of interest: S.M. Camp has nothing to disclose. Conflict of interest: J.H. Song has nothing to disclose. Conflict of interest: E. Franco has nothing to disclose. Conflict of interest: J.K. Burt has nothing to disclose. Conflict of interest: B. Sun has nothing to disclose. Conflict of interest: J.B. Mascarenhas has nothing to disclose. Conflict of interest: K. Burns has nothing to disclose. Conflict of interest: A. Gaber has nothing to disclose. Conflict of interest: R.C. Oita has nothing to disclose. Conflict of interest: V. Reyes Hernon has nothing to disclose. Conflict of interest: C. Barber has nothing to disclose. Conflict of interest: L. Moreno-Vinasco has nothing to disclose. Conflict of interest: X. Sun has nothing to disclose. Conflict of interest: A.E. Cress has nothing to disclose. Conflict of interest: D. Martin has investments in Aqualung, outside the submitted work. Conflict of interest: Z. Liu has nothing to disclose. Conflict of interest: A.A. Desai reports grants from NIH R01 (HL136603) and consultancy for Novartis, outside the submitted work. Conflict of interest: V. Natarajan has nothing to disclose. Conflict of interest: J.R. Jacobson has nothing to disclose. Conflict of interest: S.M. Dudek has nothing to disclose. Conflict of interest: C. Bime has nothing to disclose. Conflict of interest: S. Sammani has nothing to disclose. Conflict of interest: J.G.N. Garcia reports grants and non-financial support (provision of research materials) from Aqualung Therapeutics, Corp., during the conduct of the study; grants and personal fees from Aqualung Therapeutics, Corp., outside the submitted work; and has a US Patent No. 9,409,983 issued.
(Copyright ©ERS 2021.)