Manisha J. Patel
Wake Forest University
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Manisha J. Patel.
The New England Journal of Medicine | 2016
Evan J. Lipson; Serena M. Bagnasco; Jack Moore; Sekwon Jang; Manisha J. Patel; Andrea A. Zachary; Drew M. Pardoll; Janis M. Taube; Charles G. Drake
Cancers, especially skin cancers, may develop in patients undergoing solid-organ transplantation who receive long-term immunosuppression. The use of anti–PD-1 in one such patient produced an antitumor response but led to rejection of the transplanted kidney.
British Journal of Dermatology | 2002
Tamara Salam Housman; Manisha J. Patel; Fabian Camacho; Steven R. Feldman; Alan B. Fleischer; Rajesh Balkrishnan
Summary Background The Eczema Area and Severity Index (EASI) is used by dermatological investigators world‐wide to assess eczema disease severity. EASI measures are, however, time‐consuming and require trained personnel, thereby limiting its application to large‐scale epidemiological studies. Additionally, the use of self‐assessed severity indices in dermatology is restricted to adult subjects and conditions, thereby not addressing the needs of paediatric patients.
The Journal of Infectious Diseases | 2017
Lucy A McNamara; Jennifer Dolan Thomas; Jessica R. MacNeil; How Yi Chang; Michael Day; Emily Fisher; Stacey W. Martin; Tasha Poissant; Susanna Schmink; Evelene Steward-Clark; Laurel T. Jenkins; Xin Wang; Anna M. Acosta; Kristina M. Angelo; Amy Blain; Pam Cassiday; Shankar Changayil; Elizabeth Chandler Church; Kasey Diebold; Sinmisola Ewumi; Amanda Faulkner; Helen Fisun; Holly Haberman; Brian H. Harcourt; Sterling Haring; Lauren Hughes; Sandeep Joseph; Nivritti Kumaran; Adria Lee; Tanya Lennon
Background Limited data exist on the impact of the serogroup B meningococcal (MenB) vaccines MenB-FHbp and MenB-4C on meningococcal carriage and herd protection. We therefore assessed meningococcal carriage following a MenB vaccination campaign in response to a university serogroup B meningococcal disease outbreak in 2015. Methods A convenience sample of students recommended for vaccination provided oropharyngeal swab specimens and completed questionnaires during 4 carriage surveys over 11 months. Isolates were tested by real-time polymerase chain reaction analysis, slide agglutination, and whole-genome sequencing. Vaccination history was verified via university records and the state immunization registry. Results A total of 4225 oropharyngeal swab specimens from 3802 unique participants were analyzed. Total meningococcal and genotypically serogroup B carriage prevalence among sampled students were stable, at 11%-17% and 1.2%-2.4% during each round, respectively; no participants carried the outbreak strain. Neither 1-3 doses of MenB-FHbp nor 1-2 doses of MenB-4C was associated with decreased total or serogroup B carriage prevalence. Conclusions While few participants completed the full MenB vaccination series, limiting analytic power, these data suggest that MenB-FHbp and MenB-4C do not have a large, rapid impact on meningococcal carriage and are unlikely to provide herd protection in the context of an outbreak response.
Clinical Infectious Diseases | 2018
Minesh P. Shah; Patricia Quinlisk; Andrew Weigel; Jacob Riley; Lisa James; James B. Patterson; Carole J. Hickman; Paul A. Rota; Rebekah Stewart; Nakia Clemmons; Nicholas Kalas; Cristina V. Cardemil; Manisha J. Patel; Matthew Donahue; Allison Schneider; Ugochi Ukegbu; Kathleen Wittich; James A. Kellogg; Doug Beardsley; Ngoc Huu Tran; Don Callaghan; Adam Pyatt; Tricia L Kitzmann; Bethany Kintigh
Background In response to a mumps outbreak at the University of Iowa and surrounding community, university, state, and local health officials implemented a vaccination campaign targeting students <25 years of age with an additional dose of measles-mumps-rubella (MMR) vaccine. More than 4700 vaccine campaign doses were administered; 97% were documented third doses. We describe the epidemiology of the outbreak before and after the campaign, focusing on cases in university students. Methods Mumps cases were identified from reportable disease databases and university health system records. Detailed information on student cases was obtained from interviews, medical chart abstractions, university and state vaccination records, and state public health laboratory results. Pre- and postcampaign incidence among students, university faculty/staff, and community members <25 vs ≥25 years old were compared using Fisher exact test. Multivariable regression modeling was performed to identify variables associated with a positive mumps polymerase chain reaction test. Results Of 453 cases in the county, 301 (66%) occurred in university students. Student cases were primarily undergraduates (90%) and highly vaccinated (86% had 2 MMR doses, and 12% had 3 MMR doses). Fewer cases occurred in students after the campaign (75 [25%]) than before (226 [75%]). Cases in the target group (students <25 years of age) declined 9% postcampaign (P=.01). A positive mumps polymerase chain reaction test was associated with the presence of parotitis and early sample collection, and inversely associated with recent receipt of MMR vaccine. Conclusions Following a large additional dose MMR vaccination campaign, fewer mumps cases occurred overall and in the target population.
The Journal of Infectious Diseases | 2005
Phoebe D. Lu; Manisha J. Patel; Gil Yosipovitch; Aloys Cabrera; William R. Levis
1. Nalin DR. Zinc and cholera [letter]. J Infect Dis 2005; 192:1672 (in this issue). 2. Berni Canani R, Cirillo P, Buccigrossi V, et al. Zinc inhibits cholera toxin-induced, but not Escherichia coli heat-stable enterotoxin-induced, ion secretion in human enterocytes. J Infect Dis 2005; 191:1072-7. 3. Hendrickson BA, Chang EB. Intracellular mediators and mechanisms of pathogen-induced alterations in intestinal electrolyte and fluid transport. In: Blaser MJ, Smith PD, Ravdin JI, Greemberg HB, Guerrant RL, eds. Infections of the gastrointestinal tract. Lippincott Williams fc Wilkins, 2002:109-16. 4. Bhutta ZA, Bird SM, Black RE, et al. Therapeutic effects of oral zinc in acute and persistent diarrhea in children in developing countries: pooled analysis of randomized controlled trials. Am J Clin Nutr 2000;72:1516-22. 5. Ruek MT, Rivera JA, Santizo MC, et al. Impact of zinc supplementation on morbidity from diarrhea and respiratory infections among rural Guatemalan children. Pediatrics 1997; 99: 808-13. 6. Bhutta ZA, Black RE, Brown KH, et al. Prevention of diarrhea and pneumonia by zinc supplementation in children in developing countries: pooled analysis of randomized controlled trials. J Pediatr 1999; 135:689-97. 7. Baqui AH, Black RE, El Arifeen S, et al. Effect of zinc supplementation started during diarrhoea on morbidity and mortality in Bangladeshi children: community randomised trial. BMJ 2002;325:1059-62. 8. Sazawal S, Black RE, Bhan MK, et al. Zinc supplementation in young children with acute diarrhea in India. N Engl J Med 1995; 333: 839-44.
Photodermatology, Photoimmunology and Photomedicine | 2002
Michael Kucenic; Manisha J. Patel; Steven R. Feldman; Anthony Liguori; Alan B. Fleischer
Background: Visual perception has hindered the development of blinded, placebo‐controlled ultraviolet light exposure conditions in humans. New acrylic thermoplastics that block or transmit ultraviolet light have visual properties that may provide a solution.
American Journal of Dermatopathology | 2013
Nemanja Rodić; Janis M. Taube; Paul Manson; Manisha J. Patel; James W. Patterson; Gulsun Erdag
Abstract:Dermal-based combined squamous and melanocytic neoplasms are emerging clinicopathologic entities that tend to appear on sun-exposed areas of elderly patients. The biologic behavior of such cutaneous neoplasms remains uncertain because of their rarity. Histopathologic differential includes the following diagnostic entities: (1) dermal squamomelanocytic tumor, (2) melanocytic matricoma, and (3) rare histologic variant of pilomatrical carcinoma, the so-called pilomatrical carcinoma with intralesional melanocytes. Herein, we present a novel case of locally invasive dermal squamomelanocytic tumor. A 72-year-old man presented with a pigmented papule on nasal ala that was clinically concerning for basal cell carcinoma. Histopathologic evaluation demonstrated atypical melanocytic cells architecturally and intimately intermixed with single units and clusters of atypical squamous cells. Most notable feature of this case is focal matrical differentiation and locally invasive tumor growth, characterized by multifocal perineural invasion.
Handbook of Systemic Autoimmune Diseases | 2006
Manisha J. Patel; Joseph L. Jorizzo
Publisher Summary Vasculitis refers to inflammation and necrosis of blood vessels, whether they are arteries, veins or both. It can be local or systemic, and may be primary or secondary to another disease process. The classic cutaneous manifestation of vasculitis is palpable purpura; however, the clinical manifestation greatly depends on the size of the vessel affected. Leukocytoclastic vasculitis is a pathological description used to describe inflammation of post-capillary venules and is clinically more correctly termed “cutaneous small vessel vasculitis (CSVV).” CSVV occurs equally in both sexes and at all ages. It is estimated that 10% of affected patients are children. The histopathologic pattern is that of a leukocytoclastic vasculitis—angiocentric, segmental inflammation with nuclear dust, endothelial-cell swelling, and fibrinoid necrosis. The American College of Rheumatology (ACR) has proposed criteria for the diagnosis of hypersensitivity vasculitis, which corresponds to CSVV.
Journal of Cutaneous Pathology | 2007
Gary Goldenberg; Manisha J. Patel; Omar P. Sangueza; Fabian Camacho; Vishal Khanna; Steven R. Feldman
American Journal of Dermatopathology | 2006
Gary Goldenberg; Manisha J. Patel; Omar P. Sangueza; Vishal Khanna; Fabian Camacho; Christopher J. Miller; Steven R. Feldman
Collaboration
Dive into the Manisha J. Patel's collaboration.
National Center for Immunization and Respiratory Diseases
View shared research outputs