How HLA Typing Improves Immunotherapy Precision

December 6, 2023

How can HLA typing drive better immunotherapy development and selection

Immunotherapies hold enormous potential for cancer treatment, but understanding tumor–immune interactions is needed to successfully develop new therapies and identify suitable patients.

Human leucocyte antigen (HLA) typing gives deeper insights into the relationship between the immune system and cancer cells, helping scientists improve immunotherapy administration precision and develop new immunotherapeutic approaches. But what is it?

A deeper dive into HLA typing

HLAs are a combination of different single nucleotide polymorphisms (SNPs) across multiple exons. The HLA system helps the immune system distinguish between self and non-self cells by presenting antigens derived from pathogens, cancer cells, or other foreign entities to immune cells, triggering a response. HLAs are therefore pivotal in cancer immunotherapy — cancer-specific antigens are presented on HLA molecules, which T cells recognize, attack, and kill.

HLA allele and antigen composition varies significantly between individuals, however, so determining their HLA profile — HLA typing — is essential to understand disease onset, progression, and treatment.

How is HLA typing performed?

Most researchers use Sanger sequencing for HLA typing, which detects SNPs. But since both copies of the genes are sequenced together in one reaction, researchers struggle to identify whether the SNPs come from the same (cis) or the opposite (trans) chromosome, making establishing the correct HLA type difficult. Next-generation sequencing (NGS) overcomes cis/trans polymorphism ambiguities by independently identifying and amplifying individual DNA fragments for more accurate typing.

HLA typing in action

Three recent publications highlight the impact of HLA profiling in immunotherapy development:

1.    Immunotherapy in oncology

HLA type affects an individual’s susceptibility to infections or autoimmune diseases, or their oncological immunotherapy response. A 2019 publication discussed how understanding a patient’s HLA profile is vital to effectively tailor immunotherapeutic treatments. Particularly, researchers should match the HLA types of cancer patients with potential donor HLA types to improve the success of treatments like adoptive cell therapy or stem cell therapy.

HLA typing is essential in CAR T-cell therapy, where it helps in the engineering of T cells to target tumor antigens, expanding immunotherapy applications beyond standard treatments.

2.    Precision medicine

HLA genotyping can help researchers to predict the survival of HLA alleles among cancers, based on an underlying cytolytic activity (CYT) mechanism. A recent study showed that a strong HLA allele, in combination with a high tumor mutation burden, could stimulate intensive immune CYT and lead to extended HLA survival. As HLA profiles differ between patients, typing can therefore support oncologists in selecting the most appropriate immunotherapy for an individual.

3.    Viral associated cancer

The 2019 article also highlighted that carcinogenic viruses activate genes that allow cancer cells to escape immune surveillance and proliferate uncontrolled. A patient’s HLA profile plays a significant role in these immune escape mechanisms, leading to the initiation of such cancers and influencing immunotherapy response. Understanding HLA profiles can therefore help effective cancer vaccine design, improving patient outcomes.

Immunotherapy is a promising approach to treat cancers — and HLA typing is key to unlocking its potential. With HLA typing, researchers can better tailor therapies, select the right treatment, and design more effective cancer vaccines.

NGS is critical to getting clearer results from your HLA typing.

Future of HLA Typing: Artificial Intelligence and Predictive Algorithms

As HLA typing evolves, the integration of AI and machine learning is becoming key to advancing immunotherapy.

These technologies are being used to develop predictive models that combine HLA typing with tumor mutational burden (TMB), and other biomarkers, to forecast patient responses to immune checkpoint inhibitors.

This multidisciplinary approach is expected to revolutionize the personalization of cancer treatments.

At CellCarta we developed our own data analysis pipeline to evaluate immune checkpoint biomarkers by looking at RNA sequencing data.

Discover CellCarta’s genomics services.

 

About the author: 

Author photo

Nathalie Bernard (PhD) is the scientific business director for the Genomics Services unit within CellCarta. Her background is in molecular biology, and she has many years of experience in PCR and sequencing, technologies used to discover or identify DNA and RNA biomarkers of clinical utility. At CellCarta, Nathalie is using her expertise to guide our customers in finding the best solution to their genomic questions.

How HLA Typing Improves Immunotherapy Precision

December 6, 2023

How can HLA typing drive better immunotherapy development and selection

Immunotherapies hold enormous potential for cancer treatment, but understanding tumor–immune interactions is needed to successfully develop new therapies and identify suitable patients.

Human leucocyte antigen (HLA) typing gives deeper insights into the relationship between the immune system and cancer cells, helping scientists improve immunotherapy administration precision and develop new immunotherapeutic approaches. But what is it?

A deeper dive into HLA typing

HLAs are a combination of different single nucleotide polymorphisms (SNPs) across multiple exons. The HLA system helps the immune system distinguish between self and non-self cells by presenting antigens derived from pathogens, cancer cells, or other foreign entities to immune cells, triggering a response. HLAs are therefore pivotal in cancer immunotherapy — cancer-specific antigens are presented on HLA molecules, which T cells recognize, attack, and kill.

HLA allele and antigen composition varies significantly between individuals, however, so determining their HLA profile — HLA typing — is essential to understand disease onset, progression, and treatment.

How is HLA typing performed?

Most researchers use Sanger sequencing for HLA typing, which detects SNPs. But since both copies of the genes are sequenced together in one reaction, researchers struggle to identify whether the SNPs come from the same (cis) or the opposite (trans) chromosome, making establishing the correct HLA type difficult. Next-generation sequencing (NGS) overcomes cis/trans polymorphism ambiguities by independently identifying and amplifying individual DNA fragments for more accurate typing.

HLA typing in action

Three recent publications highlight the impact of HLA profiling in immunotherapy development:

1.    Immunotherapy in oncology

HLA type affects an individual’s susceptibility to infections or autoimmune diseases, or their oncological immunotherapy response. A 2019 publication discussed how understanding a patient’s HLA profile is vital to effectively tailor immunotherapeutic treatments. Particularly, researchers should match the HLA types of cancer patients with potential donor HLA types to improve the success of treatments like adoptive cell therapy or stem cell therapy.

HLA typing is essential in CAR T-cell therapy, where it helps in the engineering of T cells to target tumor antigens, expanding immunotherapy applications beyond standard treatments.

2.    Precision medicine

HLA genotyping can help researchers to predict the survival of HLA alleles among cancers, based on an underlying cytolytic activity (CYT) mechanism. A recent study showed that a strong HLA allele, in combination with a high tumor mutation burden, could stimulate intensive immune CYT and lead to extended HLA survival. As HLA profiles differ between patients, typing can therefore support oncologists in selecting the most appropriate immunotherapy for an individual.

3.    Viral associated cancer

The 2019 article also highlighted that carcinogenic viruses activate genes that allow cancer cells to escape immune surveillance and proliferate uncontrolled. A patient’s HLA profile plays a significant role in these immune escape mechanisms, leading to the initiation of such cancers and influencing immunotherapy response. Understanding HLA profiles can therefore help effective cancer vaccine design, improving patient outcomes.

Immunotherapy is a promising approach to treat cancers — and HLA typing is key to unlocking its potential. With HLA typing, researchers can better tailor therapies, select the right treatment, and design more effective cancer vaccines.

NGS is critical to getting clearer results from your HLA typing.

Future of HLA Typing: Artificial Intelligence and Predictive Algorithms

As HLA typing evolves, the integration of AI and machine learning is becoming key to advancing immunotherapy.

These technologies are being used to develop predictive models that combine HLA typing with tumor mutational burden (TMB), and other biomarkers, to forecast patient responses to immune checkpoint inhibitors.

This multidisciplinary approach is expected to revolutionize the personalization of cancer treatments.

At CellCarta we developed our own data analysis pipeline to evaluate immune checkpoint biomarkers by looking at RNA sequencing data.

Discover CellCarta’s genomics services.

 

About the author: 

Author photo

Nathalie Bernard (PhD) is the scientific business director for the Genomics Services unit within CellCarta. Her background is in molecular biology, and she has many years of experience in PCR and sequencing, technologies used to discover or identify DNA and RNA biomarkers of clinical utility. At CellCarta, Nathalie is using her expertise to guide our customers in finding the best solution to their genomic questions.

Multiplexed Mass Spec for Immunotherapy Protein Measurement

October 13, 2023

CellCarta’s poster presents a quantitative mass spectrometry workflow designed for the highly multiplexed measurement of immunomodulatory proteins to support immunotherapy clinical trials.

The workflow utilizes immuno-MRM assay panels to quantify up to 113 proteins with high sensitivity and precision, providing valuable data on immune-related biomarkers. This approach enhances the understanding of drug responses and mechanisms of action, crucial for developing new immunotherapies and combination treatments.

The method involves the use of stable-isotope-labeled peptides and immunoaffinity capture, followed by LC-MRM analysis for accurate protein quantification.

Contact us  to gain insights on advanced proteomics solutions.

View the full poster:

A Quantitative Mass Spectrometry Workflow for Highly Multiplexed Measurement of Immunomodulatory Proteins to Support Immunotherapy Clinical Trials

As presented at SITC 2023 AND EORTC 2023

Multiplexed Mass Spec for Immunotherapy Protein Measurement

October 13, 2023

CellCarta’s poster presents a quantitative mass spectrometry workflow designed for the highly multiplexed measurement of immunomodulatory proteins to support immunotherapy clinical trials.

The workflow utilizes immuno-MRM assay panels to quantify up to 113 proteins with high sensitivity and precision, providing valuable data on immune-related biomarkers. This approach enhances the understanding of drug responses and mechanisms of action, crucial for developing new immunotherapies and combination treatments.

The method involves the use of stable-isotope-labeled peptides and immunoaffinity capture, followed by LC-MRM analysis for accurate protein quantification.

Contact us  to gain insights on advanced proteomics solutions.

View the full poster:

A Quantitative Mass Spectrometry Workflow for Highly Multiplexed Measurement of Immunomodulatory Proteins to Support Immunotherapy Clinical Trials

As presented at SITC 2023 AND EORTC 2023

Accurately Predict Immune Checkpoint Inhibition Response Using Only RNA-Seq Data

June 27, 2023

  • Discover how we have improved response predictions for immune checkpoint inhibitor (ICI) therapies.
  • Explore our unique computational pipeline that defines multiple characteristics (eTMB, MSI, and more) directly from the RNA-sequencing profile of a tumor.

Accurately Predict Immune Checkpoint Inhibition Response Using Only RNA-Seq Data

June 27, 2023

  • Discover how we have improved response predictions for immune checkpoint inhibitor (ICI) therapies.
  • Explore our unique computational pipeline that defines multiple characteristics (eTMB, MSI, and more) directly from the RNA-sequencing profile of a tumor.

Oncology & Immuno-Oncology Expertise

November 5, 2021

DOWNLOAD OUR BROCHURE

OncologyExpertise-cover

Harnessing the power of biomarkers from discovery to late-stage clinical development and companion diagnostics (CDx)

Oncology & Immuno-Oncology Expertise

November 5, 2021

DOWNLOAD OUR BROCHURE

OncologyExpertise-cover

Harnessing the power of biomarkers from discovery to late-stage clinical development and companion diagnostics (CDx)

Biomarkers and Correlates in Infection and Immunity

June 26, 2020

Fast-tracking the development of treatments and ensuring early selection of a promising one depends on your ability to identify significant correlates during both pre-clinical and clinical phases.

In this webinar, we use case studies to show the importance of a multi-disciplinary systems approach in the identification of these correlates.

Understanding both pathogen and host, and their interactions, is essential to fully assess the effect of infectious diseases. The gold standard for diagnosis of an infection has been to demonstrate the presence of pathogen.

However, disease severity, progression, as well as response to treatment are often more dependent on the status of the host. Therefore, an appropriately detailed assessment of the host response will substantially inform the evaluation of antimicrobial prophylactics and therapeutics.

The immune response is complex and collaborative. A robust immune response requires multiple cell lineages and soluble factors to work in concert.

The immune response, however, can be influenced by multiple host factors including co-morbidities, levels of immune competence, type of immune response and age of the host. These factors are often meaningfully represented in specific at-risk populations and therefore need to be accounted for in development programs.

All of these factors are prevalent in the high-risk groups susceptible to the COVID19 pandemic, and age and immune function have been shown to be factors affecting vaccination generally. Furthermore, the immune correlates of protection necessary for successful vaccine development may not be the same as those required for successful therapy development.

A multi-disciplinary systems approach for the measurement of the host response is thus required to successfully address all these variables.

This presentation will support this argument by drawing examples from our extensive previous experience identifying infectious disease biomarkers in pre-clinical and clinical trial settings for diagnostic, disease progression, or treatment response applications using a variety of platforms.

The case studies will survey the identification of predictive biomarkers of disease progression and response to vaccination, as well as cellular and soluble protein correlates of vaccine response.

Speaker: Eustache Paramithiotis PhD, Vice-President, Research & Development, Caprion Biosciences Inc.

Learn more about CellCarta.

Biomarkers and Correlates in Infection and Immunity

June 26, 2020

Fast-tracking the development of treatments and ensuring early selection of a promising one depends on your ability to identify significant correlates during both pre-clinical and clinical phases.

In this webinar, we use case studies to show the importance of a multi-disciplinary systems approach in the identification of these correlates.

Understanding both pathogen and host, and their interactions, is essential to fully assess the effect of infectious diseases. The gold standard for diagnosis of an infection has been to demonstrate the presence of pathogen.

However, disease severity, progression, as well as response to treatment are often more dependent on the status of the host. Therefore, an appropriately detailed assessment of the host response will substantially inform the evaluation of antimicrobial prophylactics and therapeutics.

The immune response is complex and collaborative. A robust immune response requires multiple cell lineages and soluble factors to work in concert.

The immune response, however, can be influenced by multiple host factors including co-morbidities, levels of immune competence, type of immune response and age of the host. These factors are often meaningfully represented in specific at-risk populations and therefore need to be accounted for in development programs.

All of these factors are prevalent in the high-risk groups susceptible to the COVID19 pandemic, and age and immune function have been shown to be factors affecting vaccination generally. Furthermore, the immune correlates of protection necessary for successful vaccine development may not be the same as those required for successful therapy development.

A multi-disciplinary systems approach for the measurement of the host response is thus required to successfully address all these variables.

This presentation will support this argument by drawing examples from our extensive previous experience identifying infectious disease biomarkers in pre-clinical and clinical trial settings for diagnostic, disease progression, or treatment response applications using a variety of platforms.

The case studies will survey the identification of predictive biomarkers of disease progression and response to vaccination, as well as cellular and soluble protein correlates of vaccine response.

Speaker: Eustache Paramithiotis PhD, Vice-President, Research & Development, Caprion Biosciences Inc.

Learn more about CellCarta.