On Sunday, April 20th 2025, starting 8:30am GMT, there will be maintenance work that will involve the website being unavailable during parts of the day. We apologize for any inconvenience this may cause and appreciate your understanding.
We noted you are experiencing viewing problems
-
Check with your IT department that JWPlatform, JWPlayer and Amazon AWS & CloudFront are not being blocked by your network. The relevant domains are *.jwplatform.com, *.jwpsrv.com, *.jwpcdn.com, jwpltx.com, jwpsrv.a.ssl.fastly.net, *.amazonaws.com and *.cloudfront.net. The relevant ports are 80 and 443.
-
Check the following talk links to see which ones work correctly:
Auto Mode
HTTP Progressive Download Send us your results from the above test links at access@hstalks.com and we will contact you with further advice on troubleshooting your viewing problems. -
No luck yet? More tips for troubleshooting viewing issues
-
Contact HST Support access@hstalks.com
-
Please review our troubleshooting guide for tips and advice on resolving your viewing problems.
-
For additional help, please don't hesitate to contact HST support access@hstalks.com
We hope you have enjoyed this limited-length demo
This is a limited length demo talk; you may
login or
review methods of
obtaining more access.
Printable Handouts
Navigable Slide Index
- Introduction
- NK cell diversity, KIR and HLA
- Natural killer cell functions
- NK cells controlled by receptors for HLA
- HLA are the most polymorphic human genes
- KIR gene number is variable
- KIR recognize epitopes of HLA molecules
- KIR 'A' haplotypes
- Maintenance of diversity in human populations
- Modern human history and 4 sample populations
- Two distinct African populations
- The Yucpa Amerindian population
- 2 common and distinct KIR haplotypes in Yucpa
- Two common KIR haplotypes in Europeans
- A and B KIR haplotypes in balance worldwide
- Keeping the balance
- Identifying specific amino acids
- Positive selection
- An unusually high frequency of HLA-C*07
- Two KIR2DL3 alleles are unique to the Yucpa
- Yucpa 2DL3*009 has reduced HLA-C*07 binding
- Khoisan population
- KIR2DL1-K44 is an allele unique to Khoisan
- 2DL1*022 has switched HLA binding specificity
- Extent of diversity in populations
- Understanding the extent of KIR/HLA diversity
- High KIR allelic diversity in Ghana and Khoisan
- Very high combinatorial diversity per-population
- Very high combinatorial diversity per-individual
- Individualized NK repertoire
- NK repertoire diversity as a quantitative trait
- Conclusions (1)
- KIR/HLA in ancient humans
- Denisova, Neanderthal and modern humans
- Sequences were mapped to reference genomes
- KIR/HLA are divergent in sequence and content
- Alternative mapping strategy
- Denisova has KIR A and B haplotypes
- KIR3DL1/S1 phylogenetics
- 3DS1*013 came from ancient humans
- Admixture introduced archaic haplotypes
- Conclusions (2)
- Acknowledgements (1)
- Acknowledgements (2)
Topics Covered
- NK cell Diversity; KIR and HLA
- Genetic variety of human immune systems
- Natural killer (NK) cell functions
- HLA and KIR polymorphism
- Genetic association with infectious disease
- Pregnancy syndromes
- Maintenance of diversity in populations
- KIR haplotypes, balancing selection, population bottlenecks, human population diversity
- Natural selection and functional variation, cell-free assays, allelic variants with altered specificities
- Extent of Diversity in Populations
- HLA/KIR compound genotypes and immune identity
- Distribution of viable KIR/HLA interactions
- KIR/HLA in Ancient Humans
- Virtual HLA/KIR genotype of Denisova and Neanderthal
- Distribution of ancient human KIR/HLA alleles in modern humans
Talk Citation
Norman, P. (2011, December 7). Population-specific evolution of natural killer cell diversity [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved April 15, 2025, from https://doi.org/10.69645/ILXZ9899.Export Citation (RIS)
Publication History
- Published on December 7, 2011
Financial Disclosures
- Dr. Paul Norman has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.