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Reciprocal role of hBD2 and hBD3 on the adaptive immune response by measuring T lymphocyte proliferation in terms of CD4 and CCR6 expression

This article has been retracted. Retraction note.
  • Nima Taefehshokr EMAIL logo , Alireza Isazadeh , Amin Oveisi , Yashar Azari Key and Sina Taefehshokr
Published/Copyright: August 11, 2018

Abstract

Background

Human β-defensins (hBD2 and hBD3) are small cationic antimicrobial peptides of innate immune system which can act as a barrier against the majority of pathogens, contributing to the host immune defence.

Objective

The aim of study is to determine whether hBD2 and hBD3 play a role in development and proliferation of human effector CD4 T cells or not. Furthermore, if enhanced proliferation is observed in the presence of hBD2 and hBD3, these data will demonstrate whether chemokine receptor type 6 (CCR6) is required to be present for this activity to occur.

Methods

In this study, we examined the effect of hBD2 and hBD3 on CD4+ T cell proliferation in CCR6+ and CCR6 T cells through co-culture of peripheral blood mononuclear cells with anti-CD3 and anti-CD28 stimulation in the presence or absence of hBD2 and hBD3. Proliferation was assessed using flow cytometry.

Results

It was demonstrated that, co-culture with hBD2 and hBD3 led to up-regulation of CD4+ T cell proliferation after 72 h whereas, CD4+ T cell proliferation was suppressed after 96 h. On the other hand, CCR6 and CCR6+ T cell proliferation was up-regulated after 72 h. But, CCR6+ only was down-regulated in the second cycle in the presence of hBD3. In contrast, after 96 h CCR6+ and CCR6 T cell proliferation was decreased.

Conclusion

Collectively, our data indicated that hBD2 and hBD3 play a positive and negative regulatory role in development and proliferation of human effector CD4+ T cells which is essential for optimal adaptive immune responses and the control of immunopathology.


Correction Note

This article has been retracted by the editors/the publisher due to suspected academic misconduct which has not been refuted by the authors.


Author Statement

  1. Research funding: Authors state no funding was involved.

  2. Conflict of interest: Authors state no conflict of interest.

  3. Informed consent: Informed consent was obtained from all participants.

  4. Ethical approval: The research related to human use complied with all the relevant national regulations and institutional policies and was performed in accordance to the tenets of the Declaration of Helsinki and this experiment (13/LO/0296) has been approved by the City Road and Hampstead NHS research ethics committee.

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Published Online: 2018-08-11

©2018 Walter de Gruyter GmbH, Berlin/Boston

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