Effect of the influenza A (H1N1) live attenuated intranasal vaccine on nitric oxide (FENO) and other volatiles in exhaled breath

被引:48
作者
Mashir, A. [1 ]
Paschke, K. M. [1 ]
van Duin, D. [2 ]
Shrestha, N. K. [2 ]
Laskowski, D. [1 ,3 ]
Storer, M. K. [4 ]
Yen-Lieberman, B. [5 ]
Gordon, S. M. [2 ]
Aytekin, M. [1 ]
Dweik, R. A. [1 ,3 ]
机构
[1] Cleveland Clin, Dept Pathobiol, Lerner Res Inst, Cleveland, OH 44195 USA
[2] Cleveland Clin, Infect Dis Med Inst, Cleveland, OH 44195 USA
[3] Cleveland Clin, Dept Pulm Allergy & Crit Care Med Resp Inst, Cleveland, OH 44195 USA
[4] Syft Technol Ltd, Christchurch, New Zealand
[5] Cleveland Clin, Dept Clin Pathol, Cleveland, OH 44195 USA
关键词
ION FLOW TUBE; MASS-SPECTROMETRY; ISOPRENE; O-2(+); SIFT; H3O+; NO+; SERIES; AIR;
D O I
10.1088/1752-7155/5/3/037107
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
For the 2009 influenza A (H1N1) pandemic, vaccination and infection control were the main modes of prevention. A live attenuated H1N1 vaccine mimics natural infection and works by evoking a host immune response, but currently there are no easy methods to measure such a response. To determine if an immune response could be measured in exhaled breath, exhaled nitric oxide (FENO) and other exhaled breath volatiles using selected ion flow tube mass spectrometry (SIFT-MS) were measured before and daily for seven days after administering the H1N1 2009 monovalent live intranasal vaccine (FluMist (R), MedImmune LLC) in nine healthy healthcare workers (age 35 +/- 7 years; five females). On day 3 after H1N1 FluMist (R) administration there were increases in FENO (MEAN +/- SEM: day 0 15 +/- 3 ppb, day 3 19 +/- 3 ppb; p < 0.001) and breath isoprene (MEAN +/- SEM: day 0 59 +/- 15 ppb, day 3 99 +/- 17 ppb; p = 0.02). MS analysis identified the greatest number of changes in exhaled breath on day 3 with 137 product ion masses that changed from baseline. The exhaled breath changes on day 3 after H1N1 vaccination may reflect the underlying host immune response. However, further work to elucidate the sources of the exhaled breath changes is necessary.
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共 30 条
[1]  
Amann A., 2005, Breath analysis for clinical diagnosis and therapeutic monitoring
[2]   ATS/ERS recommendations for standardized procedures for the online and offline measurement of exhaled lower respiratory nitric oxide and nasal nitric oxide, 2005 [J].
American Thoracic Society ;
European Respiratory Society .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2005, 171 (08) :912-930
[3]   Relationship between exhaled nitric oxide and airway hyperresponsiveness following experimental rhinovirus infection in asthmatic subjects [J].
de Gouw, HWFM ;
Grunberg, K ;
Schot, R ;
Kroes, ACM ;
Dick, EC ;
Sterk, PJ .
EUROPEAN RESPIRATORY JOURNAL, 1998, 11 (01) :126-132
[4]   Exhaled nitric oxide (NO) is reduced shortly after bronchoconstriction to direct and indirect stimuli in asthma [J].
de Gouw, HWFM ;
Hendriks, J ;
Woltman, AM ;
Twiss, IM ;
Sterk, PJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 158 (01) :315-319
[5]   INVITRO BIOSYNTHESIS OF ISOPRENE FROM MEVALONATE UTILIZING A RAT-LIVER CYTOSOLIC FRACTION [J].
DENERIS, ES ;
STEIN, RA ;
MEAD, JF .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 123 (02) :691-696
[6]   Mechanisms of nitric oxide-related antimicrobial activity [J].
Fang, FC .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (12) :2818-2825
[7]   ROLE OF NITRIC-OXIDE IN MAINTAINING VASCULAR INTEGRITY IN ENDOTOXIN-INDUCED ACUTE INTESTINAL DAMAGE IN THE RAT [J].
HUTCHESON, IR ;
WHITTLE, BJR ;
BOUGHTONSMITH, NK .
BRITISH JOURNAL OF PHARMACOLOGY, 1990, 101 (04) :815-820
[8]   Human breath isoprene and its relation to blood cholesterol levels: new measurements and modeling [J].
Karl, T ;
Prazeller, P ;
Mayr, D ;
Jordan, A ;
Rieder, J ;
Fall, R ;
Lindinger, W .
JOURNAL OF APPLIED PHYSIOLOGY, 2001, 91 (02) :762-770
[9]   INCREASED NITRIC-OXIDE IN EXHALED AIR OF NORMAL HUMAN-SUBJECTS WITH UPPER RESPIRATORY-TRACT INFECTIONS [J].
KHARITONOV, SA ;
YATES, D ;
BARNES, PJ .
EUROPEAN RESPIRATORY JOURNAL, 1995, 8 (02) :295-297
[10]   A Whole Virus Pandemic Influenza H1N1 Vaccine Is Highly Immunogenic and Protective in Active Immunization and Passive Protection Mouse Models [J].
Kistner, Otfried ;
Crowe, Brian A. ;
Wodal, Walter ;
Kerschbaum, Astrid ;
Savidis-Dacho, Helga ;
Sabarth, Nicolas ;
Falkner, Falko G. ;
Mayerhofer, Ines ;
Mundt, Wolfgang ;
Reiter, Manfred ;
Grillberger, Leopold ;
Tauer, Christa ;
Graninger, Michael ;
Sachslehner, Alois ;
Schwendinger, Michael ;
Bruehl, Peter ;
Kreil, Thomas R. ;
Ehrlich, Hartmut J. ;
Barrett, P. Noel .
PLOS ONE, 2010, 5 (02)