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1111 citation(s) found for "Wu, Robin".

Desulfovibrio legallii Prosthetic Shoulder Joint Infection and Review of Antimicrobial Susceptibility and Clinical Characteristics of Desulfovibrio Infections
Vasoo, Shawn , Mason, Erin L., Gustafson, Daniel R., Cunningham, Scott A. , Cole, Nicolynn C., Vetter, Emily A., Steinmann, Scott P. , Wilson, Walter R., Patel, Robin , Berbari, Elie F. , Henry, Nancy K., Patel, Robin , Cunningham, Scott A

Journal of Clinical Microbiology | May 22, 2014 | Volume: 52 | Issue: 8 | Pages: 3105-3110

10.1128/jcm.00083-14 | PMID 24850351 Get It

ABSTRACT We describe a case of shoulder hemiarthroplasty infection with Desulfovibrio legallii . Antimicrobial susceptibilities of 36 Desulfovibrio isolates are presented. Metronidazole and carbapenems exhibited reliable activity, although piperacillin-tazobactam did not. Eleven previous cases of Desulfovibrio infection are reviewed; most arose from a gastrointestinal tract-related source.
Reovirus Activates Human Dendritic Cells to Promote Innate Antitumor Immunity
Errington‐Mais, Fiona , Steele, Lynette P., Prestwich, Robin, Harrington, Kevin J. , Pandha, Hardev , Vidal, Laura , Bono, Johann S. de , Selby, Peter J. , Vile, Richard G. , Melcher, Alan , Coffey, Matt C. , Errington-Mais, Fiona , Melcher, Alan A , Harrington, Kevin , de Bono, Johann

The Journal of Immunology | April 23, 2014 | Volume: 180 | Issue: 9 | Pages: 6018-6026

10.4049/jimmunol.180.9.6018 | PMID 18424722 Get It

Abstract Oncolytic viruses can exert their antitumor activity via direct oncolysis or activation of antitumor immunity. Although reovirus is currently under clinical investigation for the treatment of localized or disseminated cancer, any potential immune contribution to its efficacy has not been addressed. This is the first study to investigate the ability of reovirus to activate human dendritic cells (DC), key regulators of both innate and adaptive immune responses. Reovirus induced DC maturation and stimulated the production of the proinflammatory cytokines IFN-α, TNF-α, IL-12p70, and IL-6. Activation of DC by reovirus was not dependent on viral replication, while cytokine production (but not phenotypic maturation) was inhibited by blockade of PKR and NF-κB signaling. Upon coculture with autologous NK cells, reovirus-activated DC up-regulated IFN-γ production and increased NK cytolytic activity. Moreover, short-term coculture of reovirus-activated DC with autologous T cells also enhanced T cell cytokine secretion (IL-2 and IFN-γ) and induced non-Ag restricted tumor cell killing. These data demonstrate for the first time that reovirus directly activates human DC and that reovirus-activated DC stimulate innate killing by not only NK cells, but also T cells, suggesting a novel potential role for T cells in oncolytic virus-induced local tumor cell death. Hence reovirus recognition by DC may trigger innate effector mechanisms to complement the virus’s direct cytotoxicity, potentially enhancing the efficacy of reovirus as a therapeutic agent.
Inhibition Controls for Qualitative Real-Time PCR Assays: Are They Necessary for All Specimen Matrices?
Buckwalter, Seanne P., Sloan, Lynne M., Cunningham, Scott A. , Espy, Mark J., Uhl, J. R., Jones, Mary F. , Vetter, Emily A., Mandrekar, Jayawant N. , Cockerill, Franklin R., Pritt, Bobbi S. , Patel, Robin , Wengenack, Nancy L. , Patel, Robin , Pritt, Bobbi S , Cunningham, Scott A

Journal of Clinical Microbiology | April 16, 2014 | Volume: 52 | Issue: 6 | Pages: 2139-2143

10.1128/jcm.03389-13 | PMID 24740078 Get It

ABSTRACT A retrospective analysis of 386,706 specimens representing a variety of matrix types used in qualitative real-time PCR assays determined the overall inhibition rate to be 0.87% when the inhibition control was added preextraction to 5,613 specimens and 0.01% when the inhibition control was added postextraction but preamplification in 381,093 specimens. Inhibition rates of ≤1% were found for all specimen matrix types except urine and formalin-fixed, paraffin-embedded tissue.
Streptococcus suis-Related Prosthetic Joint Infection and Streptococcal Toxic Shock-Like Syndrome in a Pig Farmer in the United States
Gomez, Eric, Kennedy, Cassie C. , Cunningham, Scott A. , Patel, Robin , Virk, Abinash, Gottschalk, Marcelo G , Virk, Abinash , Patel, Robin , Kennedy, Cassie C , Cunningham, Scott A

Journal of Clinical Microbiology | April 10, 2014 | Volume: 52 | Issue: 6 | Pages: 2254-2258

10.1128/jcm.02934-13 | PMID 24719433 Get It

ABSTRACT Streptococcus suis is an emerging swine-associated zoonotic agent that can cause meningitis and septicemia in humans. We present, to our knowledge, the first case of S. suis arthroplasty infection and streptococcal toxic shock-like syndrome due to an nonencapsulated serotype 5 strain in North America.
Detection of Prosthetic Joint Infection by Use of PCR-Electrospray Ionization Mass Spectrometry Applied to Synovial Fluid
Melendez, Dante P. , Uhl, James R., Greenwood‐Quaintance, Kerryl E. , Hanssen, Arlen D. , Sampath, Rangarajan , Patel, Robin , Patel, Robin

Journal of Clinical Microbiology | April 10, 2014 | Volume: 52 | Issue: 6 | Pages: 2202-2205

10.1128/jcm.00570-14 | PMID 24719438 Get It

ABSTRACT PCR coupled with electrospray ionization mass spectrometry applied to synovial fluid specimens had an 81% sensitivity and a 95% specificity for the diagnosis of prosthetic joint infection.
Misidentification of Neisseria polysaccharea as Neisseria meningitidis with the Use of Matrix-Assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry
Cunningham, Scott A. , Mainella, Jill M., Patel, Robin , Patel, Robin , Cunningham, Scott A

Journal of Clinical Microbiology | April 3, 2014 | Volume: 52 | Issue: 6 | Pages: 2270-2271

10.1128/jcm.00664-14 | PMID 24696027 Get It

Prosthetic Joint Infection
Tande, Aaron J. , Patel, Robin , Tande, Aaron , Patel, Robin

Clinical Microbiology Reviews | April 2, 2014 | Volume: 27 | Issue: 2 | Pages: 302-345

10.1128/cmr.00111-13 | PMID 24696437 Get It

SUMMARY Prosthetic joint infection (PJI) is a tremendous burden for individual patients as well as the global health care industry. While a small minority of joint arthroplasties will become infected, appropriate recognition and management are critical to preserve or restore adequate function and prevent excess morbidity. In this review, we describe the reported risk factors for and clinical manifestations of PJI. We discuss the pathogenesis of PJI and the numerous microorganisms that can cause this devastating infection. The recently proposed consensus definitions of PJI and approaches to accurate diagnosis are reviewed in detail. An overview of the treatment and prevention of this challenging condition is provided.
Ureaplasma parvum Prosthetic Joint Infection Detected by PCR
Larson, Joshua A., Akeson, Jeffrey W., Lowery, Kristin S., Rounds, Megan A., Sampath, Rangarajan , Patel, Robin , Farrell, John Joseph , Bonomo, Robert A. , Patel, Robin

Journal of Clinical Microbiology | March 27, 2014 | Volume: 52 | Issue: 6 | Pages: 2248-2250

10.1128/jcm.00432-14 | PMID 24671783 Get It

ABSTRACT We describe the first reported case of Ureaplasma parvum prosthetic joint infection (PJI) detected by PCR. Ureaplasma species do not possess a cell wall and are usually associated with colonization and infection of mucosal surfaces (not prosthetic material). U. parvum is a relatively new species name for certain serovars of Ureaplasma urealyticum , and PCR is useful for species determination. Our patient presented with late infection of his right total knee arthroplasty. Intraoperative fluid and tissue cultures and pre- and postoperative synovial fluid cultures were all negative. To discern the pathogen, we employed PCR coupled with electrospray ionization mass spectrometry (PCR/ESI-MS). Our patient's failure to respond to empirical antimicrobial treatment and our previous experience with PCR/ESI-MS in culture-negative cases of infection prompted us to use this approach over other diagnostic modalities. PCR/ESI-MS detected U. parvum in all samples. U. parvum -specific PCR testing was performed on all synovial fluid samples to confirm the U. parvum detection.
Estimating long‐term multivariate progression from short‐term data
Donohue, Michael , Jacqmin‐Gadda, Hélène , Goff, Mélanie Le , Thomas, Ronald G. , Raman, Rema , Gamst, Anthony, Weiner, Michael W. , Dartigues, Jean‐François , Aisen, Paul , Hsiung, Ging‐Yuek Robin , Preda, Adrian , Jicha, Gregory A. , Ponto, Laura L. Boles , Beckett, Laurel , Jack, Clifford R. , Preda, Adrian , Hsiung, Gink-Yuek , Donohue, Michael C , Jicha, Gregory A

Alzheimer's & Dementia | March 22, 2014 | Volume: 10 | Issue: 5S | Pages: No page available

10.1016/j.jalz.2013.10.003 | PMID 24656849 Get It

AbstractMotivationDiseases that progress slowly are often studied by observing cohorts at different stages of disease for short periods of time. The Alzheimer's Disease Neuroimaging Initiative (ADNI) follows elders with various degrees of cognitive impairment, from normal to impaired. The study includes a rich panel of novel cognitive tests, biomarkers, and brain images collected every 6 months for as long as 6 years. The relative timing of the observations with respect to disease pathology is unknown. We propose a general semiparametric model and iterative estimation procedure to estimate simultaneously the pathological timing and long‐term growth curves. The resulting estimates of long‐term progression are fine‐tuned using cognitive trajectories derived from the long‐term “Personnes Agées Quid” study.ResultsWe demonstrate with simulations that the method can recover long‐term disease trends from short‐term observations. The method also estimates temporal ordering of individuals with respect to disease pathology, providing subject‐specific prognostic estimates of the time until onset of symptoms. When the method is applied to ADNI data, the estimated growth curves are in general agreement with prevailing theories of the Alzheimer's disease cascade. Other data sets with common outcome measures can be combined using the proposed algorithm.AvailabilitySoftware to fit the model and reproduce results with the statistical software R is available as the grace package. ADNI data can be downloaded from the Laboratory of NeuroImaging.