免疫学方向博士职位

PhD position: Regulatory T (Treg) cell fitness (m/f/d)

Institute of Molecular Biology gGmbH (IMB) · 德国 · Mainz

原帖优先:申请材料、截止时间与资格以原帖和学校官方说明为准。

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研究内容
该项目研究的是白细胞介素-6 如何在炎症期间影响调节性 T 细胞的功能和适应性。
申请条件
需要硕士学位、良好的英语水平和两封推荐信。
待遇
提供全额资助、先进的科学技术和专业技能培训、国际化的工作环境。
申请方式
申请截止日期为 2026 年 10 月 15 日,面试将于 2027 年 1 月 18-19 日在 IMB 主持。
材料清单
  • 动机信
  • 简历
  • 证书
  • 成绩单
  • 推荐信

由 @cf/meta/llama-3.3-70b-instruct-fp8-fast 生成,博士岗判定置信度 100%。

结构化信息

截止
(Europe/Berlin) 剩 8 天
学科
免疫与微生物学
合同类型
雇佣合同
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内容更新
入职
2027-02-01
导师
Ilgiz Mufazalov
来源
DAAD PhDGermany 博士岗位与项目 · 最近核对 2026-10-07
判定依据(原文摘录)
  • is_phd
    PhD position
  • english_ok
    English as our working language
  • bachelor_ok
    Master or equivalent
原文

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PhD position: Regulatory T (Treg) cell fitness (m/f/d) Full PhD Working Language English

Location Mainz

Application Deadline 15. Oct 2026

Starting Date 01. Feb 2027

• Overview • Description • Required Documents • Application

Overview Open Positions 1

Time Span 01. Feb 2027 for 3 years

Application Deadline 15. Oct 2026

Financing yes

Type of Position Full PhD

Working Language English

Required Degree Master

Areas of study Biology, Molecular Biology, Human Biology, Biomedicine

Description Description Thinking of doing your PhD in the Life Sciences? The International PhD Programme (IPP) Mainz is offering talented scientists the chance to work on cutting edge research projects . As an IPP PhD student, you will join a community of exceptional scientists working on diverse topics ranging from how organisms age or how our DNA is repaired, to how epigenetics regulates cellular identity or neural memory. Activities and responsibilities The research group of Ilgiz Mufazalov in collaboration with Ari Waisman offers the following PhD project: Regulatory T (Treg) cells are essential for controlling immune responses and preventing excessive inflammation. Currently, they are one of the most actively investigated cell types in immunology, with growing interest in their potential for treating autoimmune and inflammatory diseases. Their importance was further highlighted by the 2025 Nobel Prize in Physiology or Medicine, which recognized discoveries concerning peripheral immune tolerance mediated by Treg cells.

Tissue inflammation is often associated with increased levels of the pro-inflammatory cytokine interleukin-6 (IL-6), which can affect the function and stability of Foxp3⁺ Treg cells. How Treg cells survive and maintain their immunosuppressive function in an inflammatory environment remains poorly understood. Understanding the natural mechanisms that allow Treg cells to adapt to inflammation could help improve Treg cell-based therapies for inflammatory and autoimmune diseases.

PhD Project: How interleukin-6 shapes regulatory T cells during inflammation

IL-6 signaling is mediated by its biologically relevant receptor, IL-6R. Our preliminary data show that IL-6R is expressed on Treg cell precursors in the thymus and on naïve mature Treg cells, but is downregulated on Treg cells at sites of inflammation. Treg cells isolated from IL-6-deficient mice, which lack IL-6 signaling during development, exhibit poor survival in IL-6-driven inflammatory conditions. These findings suggest that IL-6 signaling during Treg cell development may help establish the properties required for mature Treg cells to survive and function in inflammatory environments.

We hypothesize that Treg cells dynamically adjust their response to IL-6 during development and in peripheral tissues, allowing them to maintain immune suppression during inflammation. This regulation may involve changes in IL-6R expression and associated transcriptional and epigenetic mechanisms.

In this project, we will investigate how IL-6 signaling shapes the function and fitness of Treg cells in inflamed tissues. We will use mouse models with cytokine overproduction or cytokine/receptor deficiency, as well as spontaneous and experimentally induced inflammatory models. Treg cell transfer experiments will be used to study their survival, stability, and suppressive function. We will combine multicolor flow cytometry (FACS), mouse immunology models, and sequencing approaches to identify the cellular and molecular mechanisms that control Treg cell fitness during inflammation.

The project is strongly immunological and will provide training in experimental mouse immunology, T-cell biology, flow cytometry, and molecular approaches.

If you are interested in this project, please select Mufazalov/Waisman as your group preference in the IPP application platform. Qualification profile Are you an ambitious scientist looking to push the boundaries of research while interacting with colleagues from multiple disciplines and cultures? Then joining the IPP is your opportunity to give your scientific career a flying start! All you need is: • Master or equivalent • Interactive personality & good command of English • 2 letters of reference

We offer • Exciting, interdisciplinary projects in a lively international environment, with English as our working language • Advanced training in scientific techniques and professional skills • Access to our state-of-the-art Core Facilities and their technical expertise • Fully funded positions with financing until the completion of your thesis • A lively community ofmore than 200 PhD students from 44 different countries

For more details on the projects offered and how to apply via the online form using the apply button.

The deadline for applications is 15 October 2026. Interviews will take place at IMB in Mainz on 18+19 January 2027. Starting date: 1 February - 31 July 2027

Required Documents Required Documents • Motivation letter • CV • Certificates • Transcripts • References

Application Application

https://www.imb.de/students-postdocs/international-phd-programme/apply-to-ipp/projects-offered/ari-waisman/ilgiz-mufazalov

https://www.imb.de/phd Contact Institute of Molecular Biology gGmbH (IMB) International PhD Programme (IPP) Mainz Address Street Ackermannweg 4 Zipcode 55128 City Mainz

Contact details Web: https://www.imb.de/phd

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