Previous Page  9 / 25 Next Page
Information
Show Menu
Previous Page 9 / 25 Next Page
Page Background

Page 61

Notes:

conferenceseries

.com

Volume 8, Issue 3(Suppl)

J Allergy Ther, an open access journal

ISSN: 2155-6121

Allergy-Clinical Immunology 2017

September 07-08, 2017

September 07-08, 2017 | Edinburgh, Scotland

ALLERGY, ASTHMA & CLINICAL IMMUNOLOGY

11

th

International Conference on

Male-dominant suppressive activity of CD8+ T cells on CD4+ T cells: Assessing female-dominant

allergic airway inflammation

Tomomitsu Miyasaka

1

, Chiaki Masuda

1

, Toshiaki Kikuchi

2

, Tasuku Kawano

1

, Motoaki Takayanagi

1

and

Isao Ohno

1

1

Tohoku Medical and Pharmaceutical University, Japan

2

Niigata University, Japan

Statement of the Problem:

Bronchial asthma is more severe in females than in males after puberty because of stronger Th2-

oriented immune response in females. However, the mechanism of the sex difference in asthmatic immune response remains

unclear. CD8+ T cells play an important role in regulating the asthma immune response through their suppressive effect on

Th2 polarization within the localized lymph nodes.

Theoretical Orientation:

In the present study, we investigated the sex-specific effect of CD8+ T cells on the female-predominant

asthmatic immune responses using a mouse model.

Results:

The number of eosinophil in bronchoalveolar lavage (BAL) fluid, lung Th2 cytokine levels, and IL-4 production by

bronchial lymph node cells were significantly higher in wild-type female compared with male mice, whereas no such sex

differences were observed between cd8α-disrupted (CD8KO) male and female mice. The adaptive transfer of wild-type male,

but not female, CD8+ T cells reduced the number of inflammatory cells in the recovered BAL fluid of CD8KO male, but not

female, recipient mice. Male CD8+ T cells produced higher levels of IFN-γ than female CD8+ T cells. Treatment with anti-

IFN-γ antibody completely abrogated the sex difference in the suppressive activity of CD8+ T cells on IL-4 production from

CD4+ T cells. However, IFN-γ receptor expression on CD4+ T cells was higher in male mice than in female mice. rIFN-γ

treatment increased the proportion of IFN-γ receptor α+ CD4+ T cells in male naïve CD4+ T cells more than in female naïve

CD4+ T cells.

Conclusion & Significance:

These results suggest that female-dominant asthmatic immune responses are induced by the

reduced production of IFN-γ by CD8+ T cells and the lower expression of IFN-γ receptor on CD4+ T cells caused by exposure

to IFN-γ in females compared with males.

Biography

Tomomitsu Miyasaka completed his PhD at Tohoku University, Japan. He is an Assistant Professor at Tohoku Medical and Pharmaceutical University, Japan. His

research area is Allergy, and he is interested in determining the mechanism(s) that are responsible for the altered asthma severity by sex or related to psychological

stress.

t-miya13@tohoku-mpu.ac.jp

Tomomitsu Miyasaka et al., J Allergy Ther 2017, 8:3(Suppl)

DOI: 10.4172/2155-6121-C1-006