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Background: The rabbit infectivity test (RIT) was previously described as a highly-sensitive method for clinically detecting Treponema pallidum. But our primary study indicated this result may have changed in current antibiotics era.
Methods: By inoculating rabbits testis with cerebrospinal fluid (CSF) (n=63) and exudate from hard chancre lesions (n=13), we re-evaluated the sensitivity of RIT in modern era. All isolated T. pallidum strains from the RIT were performed for the strain type based on "CDC subtype/tp0548" method. Chi-square and Fisher's exact tests were used to determine the statistical significance of differences across data sets.
Results: Result indicated that 2 of 63 CSF (2/63, 3.17%) and 5 of 13 lesion exudate samples (5/13, 38.47%) were positive in the RIT, with a much longer time to detection for CSF samples. Only 1 of 28 samples from patients who admitted treatment with antibiotics prior to clinical exam was positive in the RIT; while 6 of 48 patients, who admitted no recent exposure to antibiotics or was unclear about the medical history, were positive in RIT. DNA sequence analysis revealed 6 strains of 14d/f subtype and one strain of 14a/f subtype.
Conclusions: In conclusions, RIT is no longer a highly sensitive method for detecting T. pallidum in clinical samples as before, and is not inadequately considered to be a reference method for measuring the sensitivity of other new methods, such as the PCR. These data represent the first reexamination of the sensitivity of RIT in the post-antibiotic era with a large clinical sample.
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http://dx.doi.org/10.1016/j.cca.2016.11.031 | DOI Listing |
Cell Death Dis
August 2025
Department of Radiation Oncology, Tianjin Medical University Cancer Institute & Hospital, Key Laboratory of Cancer Prevention and Therapy, National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Tianjin, China.
Radiotherapy (RT)-elicited antitumor immunity serves as a pivotal mechanism in RT-mediated tumor control. The strategic integration of RT with immunotherapies, particularly immune checkpoint blockade (ICB), is revolutionizing cancer therapeutics, demonstrating remarkable clinical potential. In this context, identifying molecular targets to potentiate radioimmunotherapy (RIT) efficacy represents a critical research priority.
View Article and Find Full Text PDFCarbohydr Polym
November 2025
Department of Materials Science and Engineering, College of Science, Rochester Institute of Technology, Rochester, New York, USA.
In this current study, hydroxyethyl methacrylate (HEMA) was grafted onto corn starch (CS), proceeding with a chemical modification method to obtain modified CS (CS) with improved properties. When CS and CS were subjected to Fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR) characterisation, distinct peaks were observed in CS. During FTIR characterisation, peaks at 1714 cm and 1629 cm were observed, corresponding to CO stretching of HEMA and secondary amines, respectively.
View Article and Find Full Text PDFArch Toxicol
August 2025
Department of Experimental Pathology and Tumor Biology, Nagoya City University Graduate School of Medical Sciences, 1-Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya, 467-860, Japan.
Nonalcoholic steatohepatitis (NASH), associated with metabolic syndromes, causes fibrosis and cirrhosis, leading to hepatocellular carcinoma. Angiotensin II (ANG II) type 1 receptor (AT1R), expressed in hepatic stellate cells (HSCs), promotes cell proliferation and collagen production. Our study aimed to investigate the potential inhibitory effect and mechanism of the AT1R blocker (ARB) on NASH with fibrosis and carcinogenesis using a transgenic rat NASH model, focusing on the direct modulatory effect of ARB on the rat HSC cell line, RI-T.
View Article and Find Full Text PDFJ Infect Dis
June 2025
Biological Sciences Platform, Sunnybrook Research Institute, Toronto, ON, Canada.
Background: The main protease (Mpro) is one of the most attractive targets for antiviral drug discovery against SARS-CoV-2. Mutations in Mpro have been linked to resistance against nirmatrelvir-ritonavir (NIR-RIT), an important therapy for SARS-CoV-2 infection. This study aimed to identify low-frequency antiviral resistance mutations in Mpro from NIR-RIT-treated patients and to analyze the enzymatic properties, inhibitor susceptibility, and structural features of new Mpro clinical variants.
View Article and Find Full Text PDFImmunopharmacol Immunotoxicol
August 2025
Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town, South Africa.
Objective: The study aims to develop a novel recombinant anti-LGR5 immunotoxin candidate based on a truncated form of exotoxin A (ETA).
Methods: To develop this LGR5-specific recombinant immunotoxin, a corresponding single chain antibody fragment (αLGR5(scFv)) fused to ETA, was expressed under osmotic stress in the presence of compatible solutes in BL21 DE3 cells. Expression was monitored by Western blot analysis facilitated by an N-terminal 10x-His tag.