Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Michael E. Martin is active.

Publication


Featured researches published by Michael E. Martin.


The Journal of Allergy and Clinical Immunology | 1990

Allergic Bipolaris sinusitis: Clinical and immunopathologic characteristics

David S. Gourley; Bonnie A. Whisman; Neil L. Jorgensen; Michael E. Martin; Michael J. Reid

Allergic Aspergillus sinusitis was first reported in 1983. We present the first three cases of allergic fungal sinusitis caused by the black fungus Bipolaris spicifera. The patients were young, atopic, and immunocompetent. All three patients demonstrated pansinusitis with nasal polyps and underwent multiple surgical procedures. Pathologic features included a characteristic mucoid exudate containing eosinophils, Charcot-Leyden crystals, and fungal hyphae. In two cases there was bony erosion revealed by computed tomography scan but no histologic evidence of direct fungal invasion into the mucosa or bony trabeculae. Immunologic features, including total eosinophil count, total serum IgE, immediate and late-phase skin response to B. spicifera, serum precipitins, and specific IgE and IgG to B. spicifera, are described. B. spicifera is a previously unrecognized cause of allergic fungal sinusitis that may be an underdiagnosed disorder. This diagnosis should be considered in atopic patients with nasal polyps and pansinusitis unresponsive to conventional medical therapy. Diagnostic criteria include characteristic histologic allergic mucin, culture identification of fungus, positive immediate cutaneous reactivity to fungal extract, positive serum precipitins, and elevated specific IgE and IgG antibodies.


The Journal of Allergy and Clinical Immunology | 1992

Imported fire ant immunotherapy: Effectiveness of whole body extracts☆

Theodore M. Freeman; Robert Hylander; Anna Ortiz; Michael E. Martin

The purpose of this study was to determine if whole body extract (WBE) immunotherapy for imported fire ant (IFA) hypersensitivity is effective. This evaluation was carried out by retrospectively interviewing 76 patients with a history of generalized allergic reactions to IFA stings and positive skin tests to IFA-WBE. The study groups consisted of 65 patients on immunotherapy and 11 similar patients who were not treated for various reasons. In addition, an IFA sting challenge was performed in 30 volunteers of the 65 patients on immunotherapy. The retrospective review showed that of the 65 patients on immunotherapy there had been 112 subsequent field-sting episodes in 47 patients. Only one sting episode in this group (2.1%) produced an anaphylactic reaction. Six of the 11 patients not on immunotherapy have had subsequent field re-sting episodes, and each has had a systemic reaction. Repeat skin testing on 31 of the 65 patients in the immunotherapy group showed persistent positive responses in five (16%), but each was at a lower dilution than initially. Responses of the other 26 of the 31 patients who had skin testing had become negative. The four untreated patients who were available for skin testing continued to have positive responses at comparable dilutions on skin testing. Sting challenges carried out on 30 volunteers from the 65 patients (all from the 31 who had repeat skin tests) on immunotherapy resulted in only local reactions.(ABSTRACT TRUNCATED AT 250 WORDS)


The Journal of Allergy and Clinical Immunology | 1989

Suppression of the late cutaneous response by immunotherapy

John A. Fling; Michael E. Ruff; William A. Parker; Bonnie A. Whisman; Michael E. Martin; Richard B. Moss; Michael J. Reid

In a prospective, double-blind, placebo-controlled study, we examined the effect of mountain cedar (MC) immunotherapy on the MC-induced late cutaneous response (LCR). Fourteen MC-sensitive patients were intradermally skin tested before and after immunotherapy with MC extract. We measured the size of the wheal at 15 minutes and the area of tissue swelling at 6 hours. Patients were matched by the size of the LCR and started receiving either MC immunotherapy or placebo immunotherapy. MC-specific immunoglobulins (MC sIgG, MC sIgG1, MC sIgG4, and MC sIgE) were measured by ELISA. Symptom-medication scores (SMSs) were recorded on a daily basis during the MC season and tabulated at the end of the study. Comparison of the 14 paired patients revealed no significant differences between MC-treated and placebo-treated groups in preimmunotherapy MC sIgG1 and SIgG4. However, when MC immunotherapy was compared to placebo immunotherapy, patients receiving MC immunotherapy developed significantly higher MC sIgG1 (p less than 0.04) and MC sIgG4 (p less than 0.01) after immunotherapy. Patients receiving MC immunotherapy also demonstrated significantly greater suppression of the LCR after immunotherapy (p less than 0.005) with the postimmunotherapy LCR correlating significantly with both MC sIgG4 (rs = 0.715; p = 0.008) and cumulative dose of MC received (rs = 0.808; p = 0.004). MC sIgE was similar in both groups after immunotherapy. The reduction in SMSs in the MC-treated group did not reach significance, nor was there a correlation of SMSs with MC sIgE, sIgG, sIgG1, or sIgG4.(ABSTRACT TRUNCATED AT 250 WORDS)


The Journal of Allergy and Clinical Immunology | 1989

Prolongation of simple and choice reaction times in a double-blind comparison of twice-daily hydroxyzine versus terfenadine

David W. Goetz; James M. Jacobson; John E. Murnane; Michael J. Reid; Daniel W. Repperger; Chuck Goodyear; Michael E. Martin

Newer, nonsedating antihistamines provide a therapeutic alternative for the patient with allergy whose work is impaired by the side effects of traditional H1 antihistamines. To assess the differential effect of these antihistamines on reaction times and subjective symptoms, we compared terfenadine, 60 mg twice daily, to hydroxyzine, 25 mg twice daily, in a double-blind, placebo-controlled, crossover study of 16 healthy, asymptomatic adults. Simple reaction time and choice reaction time were measured with a computer-based, eye-hand, reaction-time testing apparatus. Reaction times and symptom scores were assessed 90 minutes after the fourth and tenth doses of each drug. Hydroxyzine, but not terfenadine, significantly prolonged both simple and choice reaction time (p less than or equal to 0.0001). However, decision time, the time to process one bit of spatial information, was not prolonged by either antihistamine. Therefore, hydroxyzine prolonged the interpretation and response to stimuli of the central nervous system without increasing single-bit processing time. Although terfenadine was not different from placebo for any symptom assessed, hydroxyzine produced significant drowsiness (p = 0.001), dry mouth (p = 0.022), and irritability (p = 0.021). During the 5 days of hydroxyzine administration, neither objective nor subjective symptoms demonstrated the development of tolerance. No correlation was found between subjective symptoms and prolongation of reaction times by hydroxyzine, suggesting that side effect symptoms of traditional antihistamines are unreliable predictors of objective performance. Terfenadine provides a promising therapeutic alternative to traditional antihistamines for individuals performing critical tasks.


The Journal of Allergy and Clinical Immunology | 1986

Sunflower oil is not allergenic to sunflower seed-sensitive patients

Alan B. Halsey; Michael E. Martin; Michael E. Ruff; Frank O. Jacobs; Robert L. Jacobs

The allergenicity of edible oils derived from sunflower seeds was investigated in two patients with anaphylactic sensitivity to sunflower seeds. Specific IgE-mediated hypersensitivity to sunflower seed was demonstrated by history, prick skin tests, positive passive transfer skin test, and RAST. Specific IgE directed toward sunflower oil, refined or cold pressed, could not be conclusively demonstrated. The Prausnitz-Küstner reaction with sunflower oils performed with one patients serum was negative. Although the cold-pressed sunflower oil was found to contain a minute amount of protein, open challenge with the derivative oils resulted in no immediate or delayed reaction in the two patients studied. Sunflower oil ingestion in these patients who were highly sensitive to the parent material proved safe. Nonallergenicity of derivative products needs to be proven for each case.


The Journal of Allergy and Clinical Immunology | 1983

38 The incidence of adverse reactions to foods — A continuing study

S. Allan Bock; Michael E. Martin


The Journal of Allergy and Clinical Immunology | 1988

467 Clinical and immunological characteristics of allergic fungal sinusitis caused by bipolaris spicifera

David S. Gourley; Bonnie A. Whisman; Michael E. Martin; Michael J. Reid


Pediatrics | 1984

Serum complement changes during double-blind food challenges in children with a history of food sensitivity.

Michael E. Martin; Lindsay A. Guthrie; S. Allan Bock


The Journal of Allergy and Clinical Immunology | 1991

394 Discontinuing fire ant immunotherapy

P Motta; Robert Hylander; Michael E. Martin; Theodore M. Freeman


The Journal of Allergy and Clinical Immunology | 1988

236 A placebo-controlled crossover study of simple and choice reaction times comparing terfenadine vs nightime hydroxyzine

David W. Goetz; James M. Jacobson; Michael E. Martin

Collaboration


Dive into the Michael E. Martin's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar

Bonnie A. Whisman

Wilford Hall Medical Center

View shared research outputs
Top Co-Authors

Avatar

David W. Goetz

Wright-Patterson Air Force Base

View shared research outputs
Top Co-Authors

Avatar

James M. Jacobson

Wright-Patterson Air Force Base

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Chuck Goodyear

Wright-Patterson Air Force Base

View shared research outputs
Top Co-Authors

Avatar

Daniel W. Repperger

Air Force Research Laboratory

View shared research outputs
Top Co-Authors

Avatar

John E. Murnane

Wright-Patterson Air Force Base

View shared research outputs
Top Co-Authors

Avatar

Robert L. Jacobs

University of Tennessee Health Science Center

View shared research outputs
Researchain Logo
Decentralizing Knowledge