Hao Jin, Ph.D.

Neuro-immune Crosstalk Unit

Established in 2022

NIH Main Campus, Bethesda, MD

Hao Jin, Ph.D. (He/Him/His)

Tenure Track Investigator

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Portrait of Hao Jin, Ph.D.

Major Areas of Research

  • Role of body-brain axis in the control of innate immune response
  • Representation and regulation of distinct types of immune responses by the brain
  • Modulation of immune responses by sensory experience and internal states

Program Description

The Neuro-immune Crosstalk Unit seeks to decode the multidimensional interactions between the immune and nervous systems to understand the multifaceted regulation of host immunity at the whole organismal level.

Immune responses need to be delicately regulated. Imbalance in this regulation can lead to devastating consequences. A less understood but integral dimension of immune regulation is by the nervous system. The intimacy between the immune and nervous systems occurs at many layers, conferring adaptive advantages (e.g., speed, integration and prediction) beyond the autonomous regulation by the isolated immune system. Leveraging emerging neuroscience and immunology tools, we develop and apply integrative multimodal approaches to explore these physiologically rich neuro-immune connections to unravel fundamental principles of neural control of immune responses. Currently, our research centers on the following three areas:

a) Role of body-brain axis in the control of innate immune response

We are examining how the brain monitors and alters peripheral immune responses.  We reasoned that identifying brain neurons activated by immune challenges would open unique windows into the workings of the modulation of immune responses by the brain. Recently, we have identified a neuronal population in the brainstem responsive to peripheral immune insult and showed that activating or silencing this population can bidirectionally alter immune activities. These brainstem neurons receive inputs from peripheral sensory neurons that pervasively innervate immune tissues and barrier sites. Thus, they are poised to surveille and report ongoing immune activities to the brain to drive descending immune modulatory responses. We hypothesize that this body-to-brain axis constitutes a gateway for the control of immune responses by the brain. We therefore combine multiomics, functional imaging and manipulation, and circuit cracking to decipher the cells, circuits and logic for immune sensing and regulation by the bidirectional body-brain ‘highway’.

b) Representation and regulation of distinct types of immune responses by the brain

The immune system has evolved successful immune strategies to counteract invading agents. While a fast-reacting innate response precedes a slow-arising adaptive response, adaptive responses are exquisitely tailored to incoming pathogens (e.g., Th1 or Th2 response against intracellular bacteria and viruses or parasites, respectively). Whether and how the brain customizes its top-down immune modulation according to the immunological needs of different immune responses is an open question. To answer this, we employ an arsenal of neural activity monitoring tools to compare and contrast brain-wide neural responses to categorically distinct immune challenges. This immune-to-brain mapping will then guide the design of targeted manipulation to test the roles of these brain representations and the connected circuits in modulating selective immune responses.

c) Modulation of immune responses by sensory experience and internal states

An important function of brain control of the immune system is to coordinate immune responses with other vital processes. A number of external and internal factors have been shown to influence immune responses via the brain. We are actively investigating how predictive sensory cues (either innate or learned) prime the immune system for a more effective immune response against upcoming infection.

Together, these efforts will help address fundamental questions on the functions and mechanisms of neural regulation of immunity in this emerging frontier of body-brain dialogue. We hope that our basic research on the neural modulation of immune responses would ultimately allow us to innovatively harness the unmatched power of the nervous system to combat various immune-related diseases.



Ph.D., National University of Singapore

Dr. Jin received his Bachelor of Science degree from Shanghai Jiao Tong University. He completed his Ph.D. in the National University of Singapore on the developmental biology of blood stem and immune cells. He was then trained as a postdoc in Columbia University where he switched to study the neurobiology of mammalian taste. In 2022, he began his new position as a tenure-track investigator in the Laboratory of Host Immunity and Host (LHIM) at the National Institute of Allergy and Infectious Diseases (NIAID). His research at LHIM intersects neuroscience with immunology, exploring the new frontier of the regulation of immune responses by the nervous system with an integrative multimodal approach combining contemporary neurobiology and immunobiology tools and techniques.

Selected Publications

Jin H, Fishman ZH, Ye M, Wang L, Zuker CS. Top-Down Control of Sweet and Bitter Taste in the Mammalian Brain. Cell. 2021 Jan 7;184(1):257-271.e16.

Zhang J, Jin H, Zhang W, Ding C, O'Keeffe S, Ye M, Zuker CS. Sour Sensing from the Tongue to the Brain. Cell. 2019 Oct 3;179(2):392-402.e15.

Jin H, Huang Z, Chi Y, Wu M, Zhou R, Zhao L, Xu J, Zhen F, Lan Y, Li L, Zhang W, Wen Z, Zhang Y. c-Myb acts in parallel and cooperatively with Cebp1 to regulate neutrophil maturation in zebrafish. Blood. 2016 Jul 21;128(3):415-26.

Jin H, Li L, Xu J, Zhen F, Zhu L, Liu PP, Zhang M, Zhang W, Wen Z. Runx1 regulates embryonic myeloid fate choice in zebrafish through a negative feedback loop inhibiting Pu.1 expression. Blood. 2012 May 31;119(22):5239-49.

Zhang Y, Jin H, Li L, Qin FX, Wen Z. cMyb regulates hematopoietic stem/progenitor cell mobilization during zebrafish hematopoiesis. Blood. 2011 Oct 13;118(15):4093-101.

Jin H, Xu J, Wen Z. Migratory path of definitive hematopoietic stem/progenitor cells during zebrafish development. Blood. 2007 Jun 15;109(12):5208-14.

Visit PubMed for a complete publication list.

Training Programs

NIH-Penn Immunology Graduate Partnership Program

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