Insights into causes of rare genetic immune disorders

(Press-News.org) The cellular glitches underlying a rare genetic disorder called activated PI3K Delta syndrome 2 (APDS2) have been identified by researchers at the Garvan Institute of Medical Research. The disorder is caused by genetic variations that disrupt immune cell signalling through a protein called PI3K.

“This study tells us how signalling in the immune system needs to be tightly balanced to make an effective response to infection. Sometimes it’s turned down and you have a problem, and sometimes signalling being turned up can interfere with an immune response,” says Associate Professor Elissa Deenick, Head of the Lymphocyte Signalling and Activation Lab, co-Lead of the Precision Immunology Program at Garvan and senior author of the paper.

PI3K plays a crucial role in activating immune cells for growth, proliferation, survival, migration and function. The researchers found that the genetic variations in APDS2 and a similar disorder, APDS1, alter PI3K signalling in different ways, leading to distinct effects on the immune system.

The APDS disorders are similar in their impacts but follow different genetic pathways. Variations in the PIK3R1 gene underlie APDS2, while variations in PIK3CD underlie APDS1. Though both result in increased PI3K signalling, their subtle differences – in specific cells, timescales, and mechanisms – yield distinct immune effects. In APDS2, fewer responding B cells are generated in response to vaccination, whereas in APDS1, the number of T cells is reduced. But in both cases, the disorders result in poor antibody responses. In addition, APDS2 variations appear to affect non-immune cells, resulting in growth delays.

These results also tell us about the signals that are required to achieve good vaccine responses in general. “Even for people who don’t have these two rare genetic conditions, other genes can impact these pathways – which could contribute to why different people have varied responses to vaccinations,” says Dr Tina Nguyen, co-lead author of the study and Research Officer at Garvan.

The findings reveal how finely tuned immune cell signalling must be, and how even minor disruptions can lead to immune deficiency or dysfunction. They are a significant step towards understanding the molecular processes and developing more targeted and effective treatments for the disorders.

“People with mysterious conditions often face challenges in obtaining an accurate diagnosis and understanding the root causes of their health issues. With better access to genomic testing, it’s going to become much easier for patients to receive diagnoses for conditions like APDS2. Knowing the genetic basis of a disease can enable targeted, personalised treatment plans that give patients the best chance of effective management or, hopefully over time, a cure,” says Professor Stuart Tangye, a senior investigator of the paper and Head of the Immunobiology and Immunodeficiency Lab at Garvan. 

The study was published in the Journal of Experimental Medicine.

The next step is to study how to track individual responses to treatment, developing blood tests to monitor immune health and dysfunction in order to give the right drug, at the right dose, at the right time.

--ENDS—

 

This research was supported by NHMRC Project Grants awarded to Professor Stuart Tangye and Associate Professor Elissa Deenick, and an NHMRC Investigator Grant awarded to Professor Tangye. Julia Bier was supported through The American Association of Immunologists Careers in Immunology Fellowship Program.

Associate Professor Elissa Deenick is an Associate Professor at the Faculty of Medicine and Health, UNSW Sydney. Professor Stuart Tangye is a Conjoint Professor at St Vincent's Clinical School, Faculty of Medicine and Health, UNSW Sydney.

END