B- and T-cell memory

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B- and T-cell memory

Immune system

Introduction to the immune system

Introduction to the immune system

Cytokines

Cytokines

Innate immune system

Innate immune system

Complement system

Adaptive immune system

T-cell development

B-cell development

MHC class I and MHC class II molecules

T-cell activation

B-cell activation and differentiation

Cell-mediated immunity of CD4 cells

Cell-mediated immunity of natural killer and CD8 cells

Antibody classes

Somatic hypermutation and affinity maturation

VDJ rearrangement

Contracting the immune response and peripheral tolerance

B- and T-cell memory

Anergy, exhaustion, and clonal deletion

Vaccinations

Hypersensitivity reactions

Type I hypersensitivity

Type II hypersensitivity

Type III hypersensitivity

Type IV hypersensitivity

Assessments

B- and T-cell memory

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USMLE® Step 1 questions

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High Yield Notes

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B- and T-cell memory

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Questions

USMLE® Step 1 style questions USMLE

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A patient’s immune system is exposed to a virus and subsequently forms memory B- and T cells to its antigens. One year later, the patient’s immune system is exposed to this virus again. Which of the following is true regarding the patient’s secondary immune response?

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Transcript

Content Reviewers

Rishi Desai, MD, MPH

Contributors

Gil McIntire

Evan Debevec-McKenney

Your immune system is like the military - with two main branches, the innate immune response and the adaptive immune response.

Key features of the innate immune response are that the cells are non-specific, meaning that they don’t distinguish one invader from another invader, the response is really fast - occurring within minutes to hours, and there’s no memory associated with innate responses.

The adaptive response, which is mediated by lymphocytes like B and T cells - is the opposite of the innate immune response.

B and T cells have unique receptors - the B cell receptor and T cell receptor - that differentiate pathogens from each other using their unique parts - called antigens.

These receptors are developed while the T cell or B cell is developing in the bone marrow for B cells or thymus for T cells.

Once the cell has a unique antigen-specific receptor expressed on its surface it begins traveling through the lymphatic system - passing through lymph nodes in search for the one antigen that fits the receptor perfectly.

If they encounter that antigen, a signal gets delivered to the cell’s nucleus that lead to clonal expansion.

That’s where a single T cell or B cell replicates over and over - creating an army of clones that can combat the pathogen.

Once the immune response is complete, many of these cells die by apoptosis restoring the immune response to its original size - with one major change.

Some of the B and T cells become memory cells, which are basically a pool of lymphocytes that are all set to combat the pathogen, if they encounter it again!

Immunologic memory is sometimes referred to as a secondary or anamnestic response, and it’s different from the primary response.

Summary

B and T cells are the two main types of lymphocytes or white blood cells that play a role in the immune response. Both B and T cells can remember previous encounters with foreign antigens, which helps them to quickly and effectively respond to future infections by the same microorganisms.

B cells produce antibodies, which bind to pathogens and mark them for destruction by other immune cells. T cells kill infected host cells or help B cells produce more antibodies. Memory B and T cells persist in the body for many years, providing lifelong protection against reinfection by the same pathogen.

Elsevier

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