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Article ; Online: Spherical shock waveform reconstruction by heterodyne interferometry.

Hart, Carl R / Lyons, Gregory W / White, Michael J

The Journal of the Acoustical Society of America

2024 Volume 155, Issue 1, Page(s) 769–780

Abstract: The indirect measurement of shock waveforms by acousto-optic sensing requires a method to reconstruct the field from the projected data. Under the assumption of spherical symmetry, one approach is to reconstruct the field by the Abel inversion integral ... ...

Abstract	The indirect measurement of shock waveforms by acousto-optic sensing requires a method to reconstruct the field from the projected data. Under the assumption of spherical symmetry, one approach is to reconstruct the field by the Abel inversion integral transform. When the acousto-optic sensing modality measures the change in optical phase difference time derivative, as for a heterodyne Mach-Zehnder interferometer, e.g., a laser Doppler vibrometer, the reconstructed field is the fluctuating refractive index time derivative. A technique is derived that reconstructs the fluctuating index directly by assuming plane wave propagation local to a probe beam. With synthetic data, this approach is compared to the Abel inversion integral transform and then applied to experimental data of laser-induced shockwaves. Time waveforms are reconstructed with greater accuracy except for the tail of the waveform that maps spatially to positions near a virtual origin. Furthermore, direct reconstruction of the fluctuating index field eliminates the required time integration and results in more accurate shock waveform peak values, rise times, and positive phase duration.
Language	English
Publishing date	2024-01-29
Publishing country	United States
Document type	Journal Article
ZDB-ID	219231-7
ISSN	1520-8524 ; 0001-4966
ISSN (online)	1520-8524
ISSN	0001-4966
DOI	10.1121/10.0024520
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Article ; Online: CXCL17 induces activation of human mast cells via MRGPRX2.

Ding, Jie / Hillig, Christina / White, Carl W / Fernandopulle, Nithya A / Anderton, Holly / Kern, Johannes S / Menden, Michael P / Mackay, Graham A

Allergy

2024

Language	English
Publishing date	2024-01-26
Publishing country	Denmark
Document type	Journal Article
ZDB-ID	391933-x
ISSN	1398-9995 ; 0105-4538
ISSN (online)	1398-9995
ISSN	0105-4538
DOI	10.1111/all.16036
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Article ; Online: Rice-Body Synovitis, Foreign Body Reaction, and Rotator Cuff Failure After Subacromial Balloon Spacer Augmentation of a Rotator Cuff Repair: A Case Report.

Fury, Matthew S / Cirino, Carl M / White, Alex E / Bauer, Thomas W / Taylor, Samuel A

JBJS case connector

2023 Volume 13, Issue 2

Abstract: Case: A 66-year-old woman presented with shoulder pain and weakness 4 months after augmentation of a rotator cuff repair with a Stryker InSpace subacromial balloon spacer. A magnetic resonance imaging (MRI) demonstrated a failed rotator cuff repair, ... ...

Abstract	Case: A 66-year-old woman presented with shoulder pain and weakness 4 months after augmentation of a rotator cuff repair with a Stryker InSpace subacromial balloon spacer. A magnetic resonance imaging (MRI) demonstrated a failed rotator cuff repair, large effusion with rice bodies, synovitis, axillary lymphadenopathy, loose anchors, and erosive changes to the greater tuberosity. Arthroscopy revealed balloon fragmentation surrounded by diffusely hyperemic synovium without repairable cuff tissue. Final cultures proved negative for infection. Histologic evaluation revealed ulcerated synovium with diffuse chronic and focal acute inflammation. Conclusion: Despite promising early results, augmentation of a rotator cuff repair with a subacromial balloon spacer introduces a risk of inflammatory reaction that may mimic a deep infection and compromise rotator cuff healing.
MeSH term(s)	Female ; Humans ; Aged ; Rotator Cuff/diagnostic imaging ; Rotator Cuff/surgery ; Rotator Cuff Injuries/diagnostic imaging ; Rotator Cuff Injuries/surgery ; Arthroscopy/adverse effects ; Arthroscopy/methods ; Synovitis ; Foreign-Body Reaction
Language	English
Publishing date	2023-05-26
Publishing country	United States
Document type	Case Reports ; Journal Article
ISSN	2160-3251
ISSN (online)	2160-3251
DOI	e23.00009
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Article ; Online: Supporting the Health Care Transition From Adolescence to Adulthood in the Medical Home.

White, Patience H / Cooley, W Carl

Pediatrics

2018 Volume 142, Issue 5

Abstract: Risk and vulnerability encompass many dimensions of the transition from adolescence to adulthood. Transition from pediatric, parent-supervised health care to more independent, patient-centered adult health care is no exception. The tenets and algorithm ... ...

Abstract	Risk and vulnerability encompass many dimensions of the transition from adolescence to adulthood. Transition from pediatric, parent-supervised health care to more independent, patient-centered adult health care is no exception. The tenets and algorithm of the original 2011 clinical report, "Supporting the Health Care Transition from Adolescence to Adulthood in the Medical Home," are unchanged. This updated clinical report provides more practice-based quality improvement guidance on key elements of transition planning, transfer, and integration into adult care for all youth and young adults. It also includes new and updated sections on definition and guiding principles, the status of health care transition preparation among youth, barriers, outcome evidence, recommended health care transition processes and implementation strategies using quality improvement methods, special populations, education and training in pediatric onset conditions, and payment options. The clinical report also includes new recommendations pertaining to infrastructure, education and training, payment, and research.
MeSH term(s)	Adolescent ; Adult ; Child ; Delivery of Health Care/methods ; Humans ; Patient-Centered Care/methods ; Practice Guidelines as Topic ; Quality Improvement ; Transition to Adult Care ; United States ; Young Adult
Language	English
Publishing date	2018-10-22
Publishing country	United States
Document type	Journal Article ; Technical Report
ZDB-ID	207677-9
ISSN	1098-4275 ; 0031-4005
ISSN (online)	1098-4275
ISSN	0031-4005
DOI	10.1542/peds.2018-2587
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Article ; Online: Analysis of sodium 2-mercaptoethane sulfonate in rat plasma using high performance liquid chromatography tandem-mass spectrometry.

Donkor, Abigail B / White, Carl W / Nick, Heidi J / Logue, Brian A

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences

2021 Volume 1189, Page(s) 123088

Abstract: Sodium 2-mercaptoethane sulfonate (MESNA) is a thiol-containing compound that has proven to be effective in inactivating acrolein, the toxic metabolite of some anti-cancer drugs (e.g., cyclophosphamide and ifosphamide). Also, it scavenges free radicals ... ...

Abstract	Sodium 2-mercaptoethane sulfonate (MESNA) is a thiol-containing compound that has proven to be effective in inactivating acrolein, the toxic metabolite of some anti-cancer drugs (e.g., cyclophosphamide and ifosphamide). Also, it scavenges free radicals which cause numerous disorders by attacking biological molecules. Current methods available to analyze MESNA in biological matrices include colorimetry and high-performance liquid chromatography (HPLC) with ultraviolet, fluorescence, or electrochemical detection. These methods have several limitations including low sensitivity, poor selectivity, a high degree of difficulty, and long analysis times. Hence, a rapid, simple, and sensitive HPLC tandem mass spectrometry (MS/MS) method was developed and validated to quantify MESNA in rat plasma following IP administration. The analysis of MESNA was accomplished via plasma protein precipitation, centrifugation, supernatant evaporation, reconstitution, and HPLC-MS/MS analysis. The method showcases an outstanding limit of detection (20 nM), excellent linearity (R
MeSH term(s)	Animals ; Chromatography, High Pressure Liquid/methods ; Drug Stability ; Limit of Detection ; Linear Models ; Male ; Mesna/blood ; Rats ; Rats, Sprague-Dawley ; Reproducibility of Results ; Tandem Mass Spectrometry/methods
Chemical Substances	Mesna (NR7O1405Q9)
Language	English
Publishing date	2021-12-22
Publishing country	Netherlands
Document type	Journal Article
ZDB-ID	1180823-8
ISSN	1873-376X ; 0378-4347 ; 1570-0232 ; 1387-2273
ISSN (online)	1873-376X
ISSN	0378-4347 ; 1570-0232 ; 1387-2273
DOI	10.1016/j.jchromb.2021.123088
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Article ; Online: Favipiravir and Ribavirin protect immunocompetent mice from lethal CCHFV infection.

Tipih, Thomas / Meade-White, Kimberly / Rao, Deepashri / Bushmaker, Trenton / Lewis, Mathew / Shaia, Carl / Feldmann, Heinz / Hawman, David W

Antiviral research

2023 Volume 218, Page(s) 105703

Abstract: Crimean-Congo hemorrhagic fever virus (CCHFV) causes Crimean-Congo hemorrhagic fever (CCHF) in humans with high morbidity and mortality. Currently, there is neither an approved antiviral drug nor a vaccine against CCHFV. In this study, we describe a ... ...

Abstract	Crimean-Congo hemorrhagic fever virus (CCHFV) causes Crimean-Congo hemorrhagic fever (CCHF) in humans with high morbidity and mortality. Currently, there is neither an approved antiviral drug nor a vaccine against CCHFV. In this study, we describe a lethal model of CCHFV infection using a mouse-adapted strain of CCHFV (MA-CCHFV) in adult wild-type male mice. Infected mice developed high viral loads, tissue pathology, and inflammatory immune responses before ultimately succumbing to the infection. We used the model to evaluate the protective efficacy of nucleoside analogs monulpiravir, favipiravir, ribavirin, the antibiotic tigecycline and the corticosteroids dexamethasone and methylprednisolone against lethal CCHFV infection. Tigecycline, monulpiravir and the corticosteroids failed to protect mice from lethal MA-CCHFV infection. In contrast, favipiravir and ribavirin protected animals from clinical disease and death even when treatment was delayed. Despite demonstrating uniform protection, CCHFV RNA persisted in survivors treated with favipiravir and ribavirin. Nevertheless, the study demonstrated the anti-CCHFV efficacy of favipiravir and ribavirin in a model with intact innate immunity and establishes this model for continued development of CCHFV countermeasures.
MeSH term(s)	Humans ; Male ; Animals ; Mice ; Hemorrhagic Fever Virus, Crimean-Congo/genetics ; Ribavirin/pharmacology ; Ribavirin/therapeutic use ; Hemorrhagic Fever, Crimean ; Tigecycline/therapeutic use ; Adrenal Cortex Hormones/therapeutic use
Chemical Substances	Ribavirin (49717AWG6K) ; favipiravir (EW5GL2X7E0) ; Tigecycline (70JE2N95KR) ; Adrenal Cortex Hormones
Language	English
Publishing date	2023-08-21
Publishing country	Netherlands
Document type	Journal Article ; Research Support, N.I.H., Intramural
ZDB-ID	306628-9
ISSN	1872-9096 ; 0166-3542
ISSN (online)	1872-9096
ISSN	0166-3542
DOI	10.1016/j.antiviral.2023.105703
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Article ; Online: Single dose, dual antigen RNA vaccines protect against lethal Crimean-Congo haemorrhagic fever virus infection in mice.

Leventhal, Shanna S / Meade-White, Kimberly / Shaia, Carl / Tipih, Thomas / Lewis, Mathew / Mihalakakos, Evan A / Hinkley, Troy / Khandhar, Amit P / Erasmus, Jesse H / Feldmann, Heinz / Hawman, David W

EBioMedicine

2024 Volume 101, Page(s) 105017

Abstract: Background: Crimean-Congo Haemorrhagic Fever Virus is a tick-borne bunyavirus prevalent across Asia, Africa, the Middle East, and Europe. The virus causes a non-specific febrile illness which may develop into severe haemorrhagic disease. To date, there ... ...

Abstract	Background: Crimean-Congo Haemorrhagic Fever Virus is a tick-borne bunyavirus prevalent across Asia, Africa, the Middle East, and Europe. The virus causes a non-specific febrile illness which may develop into severe haemorrhagic disease. To date, there are no widely approved therapeutics. Recently, we reported an alphavirus-based replicon RNA vaccine which expresses the CCHFV nucleoprotein (repNP) or glycoprotein precursor (repGPC) and is protective against lethal disease in mice. Methods: Here, we evaluated engineered GPC constructs to find the minimal enhancing epitope of repGPC and test two RNA vaccine approaches to express multiple antigens in vivo to optimize protective efficacy of our repRNA. Findings: Vaccination with repNP and a construct expressing just the Gc antigen (repGc-FL) resulted in equivalent immunogenicity and protective efficacy compared to original repNP + repGPC vaccination. This vaccine was protective when prepared in either of two vaccine approaches, a mixed synthesis reaction producing two RNAs in a single tube and a single RNA expressing two antigens. Interpretation: Overall, our data illustrate two vaccine approaches to deliver two antigens in a single immunization. Both approaches induced protective immune responses against CCHFV in this model. These approaches support their continued development for this and future vaccine candidates for CCHFV and other vaccines where inclusion of multiple antigens would be optimal. Funding: This work was supported by the Intramural Research Program, NIAID/NIH, HDT Bio and MCDC Grant #MCDC2204-011.
MeSH term(s)	Animals ; Mice ; Hemorrhagic Fever Virus, Crimean-Congo/genetics ; mRNA Vaccines ; Hemorrhagic Fever, Crimean/prevention & control ; Vaccines ; Vaccination
Chemical Substances	mRNA Vaccines ; Vaccines
Language	English
Publishing date	2024-02-20
Publishing country	Netherlands
Document type	Journal Article
ZDB-ID	2851331-9
ISSN	2352-3964
ISSN (online)	2352-3964
DOI	10.1016/j.ebiom.2024.105017
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Article ; Online: Mesna Improves Outcomes of Sulfur Mustard Inhalation Toxicity in an Acute Rat Model.

Nick, Heidi J / Johnson, Carly A / Stewart, Amber R / Christeson, Sarah E / Bloomquist, Leslie A / Appel, Amanda S / Donkor, Abigail B / Veress, Livia A / Logue, Brian A / Bratcher, Preston E / White, Carl W

The Journal of pharmacology and experimental therapeutics

2024 Volume 388, Issue 2, Page(s) 576–585

Abstract: Inhalation of high levels of sulfur mustard (SM), a potent vesicating and alkylating agent used in chemical warfare, results in acutely lethal pulmonary damage. Sodium 2-mercaptoethane sulfonate (mesna) is an organosulfur compound that is currently Food ... ...

Abstract	Inhalation of high levels of sulfur mustard (SM), a potent vesicating and alkylating agent used in chemical warfare, results in acutely lethal pulmonary damage. Sodium 2-mercaptoethane sulfonate (mesna) is an organosulfur compound that is currently Food and Drug Administration (FDA)-approved for decreasing the toxicity of mustard-derived chemotherapeutic alkylating agents like ifosfamide and cyclophosphamide. The nucleophilic thiol of mesna is a suitable reactant for the neutralization of the electrophilic group of toxic mustard intermediates. In a rat model of SM inhalation, treatment with mesna (three doses: 300 mg/kg intraperitoneally 20 minutes, 4 hours, and 8 hours postexposure) afforded 74% survival at 48 hours, compared with 0% survival at less than 17 hours in the untreated and vehicle-treated control groups. Protection from cardiopulmonary failure by mesna was demonstrated by improved peripheral oxygen saturation and increased heart rate through 48 hours. Additionally, mesna normalized arterial pH and pACO
MeSH term(s)	Rats ; Animals ; Mustard Gas/toxicity ; Mesna/pharmacology ; Mesna/therapeutic use ; Antidotes/pharmacology ; Antidotes/therapeutic use ; Lung ; Sodium ; Chemical Warfare Agents/toxicity
Chemical Substances	Mustard Gas (T8KEC9FH9P) ; Mesna (NR7O1405Q9) ; Antidotes ; Sodium (9NEZ333N27) ; Chemical Warfare Agents
Language	English
Publishing date	2024-01-17
Publishing country	United States
Document type	Journal Article ; Research Support, N.I.H., Extramural
ZDB-ID	3106-9
ISSN	1521-0103 ; 0022-3565
ISSN (online)	1521-0103
ISSN	0022-3565
DOI	10.1124/jpet.123.001683
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Article ; Online: CXCL17 is an allosteric inhibitor of CXCR4 through a mechanism of action involving glycosaminoglycans.

White, Carl W / Platt, Simon / Kilpatrick, Laura E / Dale, Natasha / Abhayawardana, Rekhati S / Dekkers, Sebastian / Kindon, Nicholas D / Kellam, Barrie / Stocks, Michael J / Pfleger, Kevin D G / Hill, Stephen J

Science signaling

2024 Volume 17, Issue 828, Page(s) eabl3758

Abstract: CXCL17 is a chemokine principally expressed by mucosal tissues, where it facilitates chemotaxis of monocytes, dendritic cells, and macrophages and has antimicrobial properties. CXCL17 is also implicated in the pathology of inflammatory disorders and ... ...

Abstract	CXCL17 is a chemokine principally expressed by mucosal tissues, where it facilitates chemotaxis of monocytes, dendritic cells, and macrophages and has antimicrobial properties. CXCL17 is also implicated in the pathology of inflammatory disorders and progression of several cancers, and its expression is increased during viral infections of the lung. However, the exact role of CXCL17 in health and disease requires further investigation, and there is a need for confirmed molecular targets mediating CXCL17 functional responses. Using a range of bioluminescence resonance energy transfer (BRET)-based assays, here we demonstrated that CXCL17 inhibited CXCR4-mediated signaling and ligand binding. Moreover, CXCL17 interacted with neuropillin-1, a VEGFR2 coreceptor. In addition, we found that CXCL17 only inhibited CXCR4 ligand binding in intact cells and demonstrated that this effect was mimicked by known glycosaminoglycan binders, surfen and protamine sulfate. Disruption of putative GAG binding domains in CXCL17 prevented CXCR4 binding. This indicated that CXCL17 inhibited CXCR4 by a mechanism of action that potentially required the presence of a glycosaminoglycan-containing accessory protein. Together, our results revealed that CXCL17 is an endogenous inhibitor of CXCR4 and represents the next step in our understanding of the function of CXCL17 and regulation of CXCR4 signaling.
MeSH term(s)	Chemokines, CXC/metabolism ; Glycosaminoglycans/pharmacology ; Ligands ; Chemokines/metabolism ; Signal Transduction ; Receptors, CXCR4/genetics ; Chemokine CXCL12
Chemical Substances	Chemokines, CXC ; Glycosaminoglycans ; Ligands ; Chemokines ; Receptors, CXCR4 ; Chemokine CXCL12
Language	English
Publishing date	2024-03-19
Publishing country	United States
Document type	Journal Article
ZDB-ID	2417226-1
ISSN	1937-9145 ; 1945-0877
ISSN (online)	1937-9145
ISSN	1945-0877
DOI	10.1126/scisignal.abl3758
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Article: Analysis of sodium 2-mercaptoethane sulfonate in rat plasma using high performance liquid chromatography tandem-mass spectrometry

Donkor, Abigail B. / White, Carl W. / Nick, Heidi J. / Logue, Brian A.

Journal of chromatography. 2022 Jan. 15, v. 1189

2022

Abstract	Sodium 2-mercaptoethane sulfonate (MESNA) is a thiol-containing compound that has proven to be effective in inactivating acrolein, the toxic metabolite of some anti-cancer drugs (e.g., cyclophosphamide and ifosphamide). Also, it scavenges free radicals which cause numerous disorders by attacking biological molecules. Current methods available to analyze MESNA in biological matrices include colorimetry and high-performance liquid chromatography (HPLC) with ultraviolet, fluorescence, or electrochemical detection. These methods have several limitations including low sensitivity, poor selectivity, a high degree of difficulty, and long analysis times. Hence, a rapid, simple, and sensitive HPLC tandem mass spectrometry (MS/MS) method was developed and validated to quantify MESNA in rat plasma following IP administration. The analysis of MESNA was accomplished via plasma protein precipitation, centrifugation, supernatant evaporation, reconstitution, and HPLC-MS/MS analysis. The method showcases an outstanding limit of detection (20 nM), excellent linearity (R² = 0.999, and percent residual accuracy >90%) and a wide linear range (0.05–200 μM). The method also produced good accuracy and precision (100 ± 10% and <10% relative standard deviation, respectively). The validated method was successfully used to analyze MESNA from treated animals and will allow easier development of MESNA for therapeutic purposes.
Keywords	acrolein ; blood proteins ; centrifugation ; colorimetry ; cyclophosphamide ; detection limit ; electrochemistry ; evaporation ; fluorescence ; high performance liquid chromatography ; metabolites ; rats ; sodium ; standard deviation ; sulfonates ; tandem mass spectrometry ; therapeutics ; toxicity
Language	English
Dates of publication	2022-0115
Publishing place	Elsevier B.V.
Document type	Article
ISSN	1570-0232
DOI	10.1016/j.jchromb.2021.123088
Database	NAL-Catalogue (AGRICOLA)

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