We have an exciting new #preprint on @medrxivpreprint ! A novel class of #primaryimmunodeficiency, with the discovery of ITPR3 mutations in two families with combined immunodeficiency. As always, studying #PID teaches us so much about biology! 1/8

medrxiv.org/content/10.110…
The work is based on patients identified @UZLeuven by Rik Schrijvers and @IsabelleMeyts. Both patients had a combined #immunodeficiency with sensitivity to infections, one complicated by peripheral #neuropathy and one by #autoimmune hemolytic anemia. Over to the gene hunters! 2/8
Mutations in ITPR3 were identified by Erika Van Nieuwenhove and Frederik Staels. ITPR3 is part of a #Calcium channel, so we turned to the Serysheva lab @Irina52948708 to predict the impact on structure. Clear as day, the mutations change the charge of the channel. 3/8
Collaborating with Lara Terry and David Yule @UofR let us calculate the exact functional defect caused by this mutation: it is 100-fold less efficient at transporting #Calcium signals than the wildtype allele. 4/8
So lucky to have a world leader in Calcium signalling at @LeuvenU, with Geert Bultynck. The incredibly talented @JulikaNeumann was able to develop new methods with @LMCSLeuven to measure the defect that patient #whitebloodcells have in responding to activation. 5/8
Why does this matter? #Calcium is like #WiFi. Your smartphone is crippled without data, #whitebloodcells are crippled without #Calcium channels. Our patients have all the #whitebloodcells they need, but without #signalling they just sit there while infections rage! 6/8
Thankfully our clinical friends could treat both patients. One required a bone-marrow transplant, as their #whitebloodcells were just ignoring all signals. The other has a more mild mutation (their cells are just hard-of-hearing), and is doing well with antibody transfusion. 7/8
Thanks to @VIBLifeSciences, @KU_Leuven, @EU_H2020 and @BBSRC for funding, and @JulikaNeumann and Stephanie Humblet-Baron for leadership.
Due to this project we can identify and treat new #PID patients, and we know more about how #whitebloodcells work in healthy individuals. 8/8

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More from @LabListon

1 Jul 20
I am really thrilled to release #AutoSpill onto @biorxivpreprint. It is a novel method for applying compensation to #flowcytometry data, which reduces the error by ~100,000-fold. It is thanks to AutoSpill that we can push machines to their max colours

biorxiv.org/content/10.110…
#AutoSpill is a beautiful example of what #maths can add to #immunology, led by the talented Dr Carlos Roca.

It has really open up my eyes to the potential of #computationalbiology, and is the reason why we have a new #datascience position available:

babrahaminstitute.livevacancies.co.uk/#/job/details/…
So how does #AutoSpill work? If you just want to compensate your data, simply upload your single colour controls to autospill.vib.be and then copy the spillover matrix to your #flowcytometry program of choice

@CarlyEWhyte can walk you through the whole process in <2'
Read 20 tweets
4 May 20
@sakisci @BetterAcademia @AcademicChatter @OpenAcademics I'm a first gen high-school graduate, now first gen PhD and professor :)

Don't be too scared off by the comments you have here. Most only really apply to the US. I'm assuming that you are doing a biomed PhD in the UK based on your profile, so a few tips... 1/n
@sakisci @BetterAcademia @AcademicChatter @OpenAcademics First, getting into a PhD program is tough. You've made it, congratulations! By definition you have the intellectual ability to finish. Never doubt that.

That said, you will doubt it. Especially at the 3-6 month period and at ~2 years in. That is normal.

2/n
@sakisci @BetterAcademia @AcademicChatter @OpenAcademics Second, it is your PhD, but the lab's project. You should aim to become the intellectual leader of the project after around a year, but always lead with humility. Others around you will always know more than you on specific techniques or domain knowledge. 3/n
Read 21 tweets

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