100% satisfaction guarantee Immediately available after payment Both online and in PDF No strings attached
logo-home
Summary SV The Immune System (Parham 4th) - Chapter 5 $3.21
Add to cart

Summary

Summary SV The Immune System (Parham 4th) - Chapter 5

1 review
 210 views  9 purchases
  • Course
  • Institution
  • Book

This English summary provides a wide overview of the subjects discussed in Parham et al. 2012 'The Immune System'. Including: T-cell production and diversity, gene recombination and MHC diversity. It contains all the important concepts and definitions of Chapter 5 and uses images to clarify.

Preview 1 out of 6  pages

  • Unknown
  • October 15, 2020
  • 6
  • 2020/2021
  • Summary

1  review

review-writer-avatar

By: mellandry • 4 year ago

avatar-seller
THE IMMUNE SYSTEM – PARHAM 4TH EDITION

CHAPTER 5

T-cell receptors (TCRs) have a similar structure to BCRs but bind mainly to peptide antigens,
derived from pathogenic proteins. This peptide is presented on human cells by a glycoprotein:
the MHC molecule.
TCR recognition of the peptide relies on peptide AND the MHC molecule

Major histocompatibility complex (MHC) = chromosomal region that encodes MHC molecules.
 Some genes are polymorphic; different variants of the same gene.

TCR structure
A TCR…
 has two polypeptide chains: TCRα and TCRβ.
Their rearrangement resembles that of immunoglobulins.
 strongly resembles the Fab fragment of an antibody: with a V- and C-region.
 contains complementarity-determining regions = CDRs.
The regions of hypervariability in TCRs are: CDR1, CDR2, CDR3.

Gene rearrangement in T-cell
The T-cell receptor only undergoes gene rearrangement during T-cell development and does
not change after an encounter with a pathogen.
The α-chain resembles the H-chain in B-cells: V-J
The β-chain resembles the L-chain in B-cells: V-D-J

RAG and DNA-modifying enzymes are involved in the recombination process.
Additional N and P nucleotides are inserted between V, (D) and J genes.
This adds to junctional diversity in the CDR3 region.

 Severe combined immunodeficiency disease = SCID = is caused by an absence of RAG enzymes; functional T- and
B-cells are absent (hence ‘combined’). Infants that do not get a bone marrow transplant, will die from SCID.
 Omenn syndrome = a mutation produces RAG with partial enzymatic activity. Patients suffer from chronic
inflammation – of the skin, a bright red rash. Without a bone marrow transplant, infants will die from this disease.
Gene rearrangement " transcription " splicing " mRNA " α-chain and β-chain to ER " α:β TCR on membrane.

RAG genes key in diversity
V(D)J recombination generates clonal diversity. Key is the two subunits of RAG recombinase.
A theory: RAG genes are transposons that are incorporated in the DNA.
Transposons can make copies of itself and move it to other parts of the chromosome.
It has transposase, an enzyme that cuts ds DNA and recognizes terminal repeat sequences.
The terminal repeat sequences evolved to be the RSSs.

The α- and β-chains need coupling with the CDR3 complex to leave the ER and form the TCR complex.
The CD3 and ζ-chain are need for intracellular signaling.
 Deficiency of the CD3δδ and CDR3δε lead to a low number of TCRs and immunodeficiency.

γ:δ TCR is a second TCR class. γ:δ T-cells reside in tissue, resemble NK cells and do not need MHC for recognition.

Gene rearrangement is similar to α:β,
but:
1) the δ- chain is on the α-chain locus
2) δ- and γ-chain have fewer genes
3) the γ- chain can include 2 D segments:
more variability

The benefits of buying summaries with Stuvia:

Guaranteed quality through customer reviews

Guaranteed quality through customer reviews

Stuvia customers have reviewed more than 700,000 summaries. This how you know that you are buying the best documents.

Quick and easy check-out

Quick and easy check-out

You can quickly pay through credit card or Stuvia-credit for the summaries. There is no membership needed.

Focus on what matters

Focus on what matters

Your fellow students write the study notes themselves, which is why the documents are always reliable and up-to-date. This ensures you quickly get to the core!

Frequently asked questions

What do I get when I buy this document?

You get a PDF, available immediately after your purchase. The purchased document is accessible anytime, anywhere and indefinitely through your profile.

Satisfaction guarantee: how does it work?

Our satisfaction guarantee ensures that you always find a study document that suits you well. You fill out a form, and our customer service team takes care of the rest.

Who am I buying these notes from?

Stuvia is a marketplace, so you are not buying this document from us, but from seller manuelavooijs. Stuvia facilitates payment to the seller.

Will I be stuck with a subscription?

No, you only buy these notes for $3.21. You're not tied to anything after your purchase.

Can Stuvia be trusted?

4.6 stars on Google & Trustpilot (+1000 reviews)

50843 documents were sold in the last 30 days

Founded in 2010, the go-to place to buy study notes for 14 years now

Start selling
$3.21  9x  sold
  • (1)
Add to cart
Added