Janine Evans
Yale University
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Publication
Featured researches published by Janine Evans.
The New England Journal of Medicine | 1998
Leonard H. Sigal; John M. Zahradnik; Philip T. Lavin; Sondra J. Patella; Gary L. Bryant; Ray Haselby; Eileen Hilton; Mark J. Kunkel; Debra Adler-Klein; Terrence Doherty; Janine Evans; Steven E. Malawista
BACKGROUND Lyme disease is a multisystem inflammatory disease caused by infection with the tick-borne spirochete Borrelia burgdorferi and is the most common vector-borne infection in the United States. We assessed the efficacy of a recombinant vaccine consisting of outer-surface protein A (OspA) without adjuvant in subjects at risk for Lyme disease. METHODS For this double-blind trial, 10,305 subjects 18 years of age or older were recruited at 14 sites in areas of the United States where Lyme disease was endemic; the subjects were randomly assigned to receive either placebo (5149 subjects) or 30 microg of OspA vaccine (5156 subjects). The first two injections were administered 1 month apart, and 7515 subjects also received a booster dose at 12 months. The subjects were observed for two seasons during which the risk of transmission of Lyme disease was high. The primary end point was the number of new clinically and serologically confirmed cases of Lyme disease. RESULTS The efficacy of the vaccine was 68 percent in the first year of the study in the entire population and 92 percent in the second year among the 3745 subjects who received the third injection. The vaccine was well tolerated. There was a higher incidence of mild, self-limited local and systemic reactions in the vaccine group, but only during the seven days after vaccination. There was no significant increase in the frequency of arthritis or neurologic events in vaccine recipients. CONCLUSIONS In this study, OspA vaccine was safe and effective in the prevention of Lyme disease.
Clinics in Chest Medicine | 2010
Danielle Antin-Ozerkis; Janine Evans; Ami N. Rubinowitz; Robert J. Homer; Richard A. Matthay
Pulmonary disease is a major source of morbidity and mortality in rheumatoid arthritis, manifesting most commonly as interstitial lung disease, airways disease, rheumatoid nodules, and pleural effusions. The diagnostic assessment of respiratory abnormalities is complicated by underlying risk for infection, the use of drugs with known pulmonary toxicity, and the frequency of lung disease related to rheumatoid arthritis itself. Evaluation and management of rheumatoid arthritis-associated pulmonary disease frequently necessitates a multidisciplinary approach.
Clinics in Chest Medicine | 2012
Danielle Antin-Ozerkis; Ami N. Rubinowitz; Janine Evans; Robert J. Homer; Richard A. Matthay
The connective tissue diseases (CTDs) are inflammatory, immune-mediated disorders in which interstitial lung disease (ILD) is common and clinically important. Interstitial lung disease may be the first manifestation of a CTD in a previously healthy patient. CTD-associated ILD frequently presents with the gradual onset of cough and dyspnea, although rarely may present with fulminant respiratory failure. Infection and drug reaction should always be ruled out. A diagnosis of idiopathic ILD should never be made without a careful search for subtle evidence of underlying CTD. Treatment of CTD-ILD typically includes corticosteroids and immunosuppressive agents.
Molecular Biology Reports | 1992
Andrew J. Griffith; Joe Craft; Janine Evans; Tsuneyo Mimori; John A. Hardin
AbstractcDNA encoding the p70 polypeptide subunit of the human Ku autoantigen was isolated. In vitro expression analysis of the cDNA demonstrates that it encodes the entire open reading frame. Nucleotide sequence analysis and comparison to other previously described sequences indicate the existence of several single-nucleotide and amino acid polymorphisms. Southern blot analyses demonstrate the presence of multiple copies of homologous DNA sequences in the human genome. These data support the hypothesis that multiple genes encode a family of Ku(p70)-related polypeptides.
Clinics in Chest Medicine | 1998
Janine Evans
This article discusses the use and interpretation of antinuclear antibody (ANA) testing in connective tissue diseases. Methods of ANA detection are discussed and analyzed in detail as is the role of ANAs in systemic lupus, scleroderma, and polymyositis, connective tissue diseases with prominent pulmonary involvement.
Interstitial Lung Disease | 2018
Danielle Antin-Ozerkis; Ami N. Rubinowitz; Janine Evans; Robert J. Homer; Richard A. Matthay
The connective tissue diseases (CTDs) are inflammatory, immune-mediated disorders in which interstitial lung disease (ILD) is common and clinically important. ILD may be the first manifestation of a CTD in a previously healthy patient. CTD-associated ILD frequently presents with the gradual onset of cough and dyspnea, although rarely may present with fulminant respiratory failure. Infection and drug reaction should always be ruled out. A diagnosis of idiopathic ILD should never be made without a careful search for subtle evidence of underlying CTD. Treatment of CTD-ILD typically includes corticosteroids and immunosuppressive agents. The authors discuss the diagnostic approach to CTD-ILD and provide a focused discussion of treatment for several common forms of CTD-ILD.
The New England Journal of Medicine | 2001
Mark S. Klempner; Linden T. Hu; Janine Evans; Christopher H. Schmid; Gary M. Johnson; Richard P. Trevino; Delona Norton; Lois Levy; Diane Wall; John McCall; Mark Kosinski; Arthur Weinstein
Arthritis & Rheumatism | 1991
Janine Evans; Adrian Reuben; Joe Craft
Archive | 2011
Minna J. Kohler; John S. Reach Msc; Janine Evans; Lawrence Weis; Joe Craft; Liana Fraenkel
Clinical Infectious Diseases | 1997
Leonard H. Sigal; D. Adler-Klein; Gary L. Bryant; T. Doherty; R. Haselby; Eileen Hilton; M. S. Klempner; Mark J. Kunkel; S. E. Malawista; Janine Evans; P. Molloy; J. Sabetta; A. Seidner; H. I. Simon; I. Mays; I. M. Zahradnik; D. Marks