Active Infection & Immunity Cells, Biochemistry & Physiology

Regulation of B cell responses to vaccines by long-term retention of antigens in germinal centres

In plain English

AI plain-English summary

Vaccines often fail because the immune system does not "see" the vaccine material long enough to produce high-quality antibodies. A team has identified a type of accessory immune cell in lymph nodes that captures and holds onto foreign material for weeks, presenting it to antibody-producing B cells. This matters because many traditional vaccines require multiple doses and still struggle to protect against rapidly mutating pathogens like flu or HIV. The researchers aim to understand exactly how these accessory cells work—what makes them hold onto antigens, and how that retention improves antibody quality. If successful, this could lead to redesigned vaccines that generate strong, lasting protection with fewer doses and faster development timelines. For the public, that means quicker responses to emerging outbreaks and better protection from complex diseases. This is fundamental science: it explores a basic mechanism of immune memory. Past discoveries in how lymph nodes process antigens have already shaped modern vaccine adjuvants, so a deeper understanding here could similarly unlock new vaccine engineering strategies.

View original technical description
Vaccines have eliminated the danger of many lethal infections and remain the best tool to combat new pathogens. However, traditional vaccines have limitations and don't protect well from rapidly changing or otherwise sophisticated pathogens. Vaccines also take time to develop and often require several doses to achieve good protection, delaying their efficacy against emerging threats. One of the possible advancements in vaccine design is to improve the entry of vaccine material into draining lymph nodes and make them persist long enough to stimulate a strong immune response. Retention of the vaccine over time is particularly important to generate protective antibodies which take several weeks to develop. We have identified a specific type of accessory immune cells that capture and keep foreign materials in lymph nodes for long periods of time (weeks) and present them to immune cells called B lymphocytes, which produce antibodies. Our main aim is to determine the properties of these accessory cells so that we can understand how the retention of foreign materials works and how it helps B lymphocytes to produce antibodies of high quality. We use the new knowledge to evaluate current vaccine properties and develop improvements to generate a stronger antibody response with a lower dosage.

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Researchers

Pavel Tolar (Principal Investigator)Shenshen Wang (Co-Investigator)

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Original classification

Research Grant

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