These T regulatory cells work by producing inhibitory cytokines (proteins such as Interleukin 10) and by cell-cell contact they send inhibitory signals
Virtually every EAE study where there is an inhibition, proposes a mechanism whereby control of EAE is associated with a loss of T reg function.
Therefore it makes you think that wouldn't it be great if our mechanism of action is associated with an increase in T regulatory function.
You make do your experiments to prove that your drug works by increasing T reg cells.
Don't believe me. Have a read of most current EAE papers. Is there a dissenting voice....not really, because they would get their paper rejected:-(.
There you have it. Alemtuzumab is associated with a reduction in CD4 T cell numbers and a relative increase in T regulatory cells. This is how alemtuzumab works!!! Yeah sorted.
So according to
They said "Prior to treatment there was no difference between patients and healthy controls in the proportion of CD4+ T cells that were CD4+CD25high. However, after Campath-1H treatment CD4+CD25high cells were significantly over-represented in the depleted CD4+ pool....This was most marked at 3 months (median of 13.5% of CD4+ T cells compared to a baseline of 3.7%, p < 0.000002..)."
So Tregs increase at least for a few months after treatment
Did anyone else find this?....Yep everyone. Even those not working in MS, it all fits the concept that Tregs control autoimmunity
Zhang X, Tao Y, Chopra M, Ahn M, Marcus KL, Choudhary N, Zhu H, Markovic-Plese S. Differential reconstitution of T cell subsets following immunodepleting treatment with alemtuzumab (anti-CD52 monoclonal antibody) in patients with relapsing-remitting multiple sclerosis. J Immunol. 2013; 191:5867-74.
Abstract "CD4(+)CD25(+)CD127(low) regulatory T cells preferentially expanded within the CD4(+) lymphocytes, reaching their peak expansion at month 1" ...from n=10
Here's another one
De Mercanti S, Rolla S, Cucci A, Bardina V, Cocco E, Vladic A, Soldo-Butkovic S, Habek M, Adamec I, Horakova D, Annovazzi P, Novelli F, Durelli L, Clerico M. Alemtuzumab long-term immunologic effect: Treg suppressor function increases up to 24 months. Neurol Neuroimmunol Neuroinflamm. 2016 ;3(1):e194.
Also said "A significant increase in Treg cell percentage was observed at month 24 and was accompanied by an increase in Treg cell suppressive activity against MBP-specific Th1 and Th17 cells".
Also Genzyme found it and bought into the idea too.
Havari E, Turner MJ, Campos-Rivera J, Shankara S, Nguyen TH, Roberts B, Siders W, Kaplan JM.Impact of alemtuzumab treatment on the survival and function of human regulatory T cells in vitro. Immunology. 2014;141(1):123-31.
"The mean percentage of Foxp3+ CD4+ T cells was 46·5 ± 3·9% in the alemtuzumab-exposed group compared with 3·8 ± 0·4% in the control IgG group, amounting to an average 13-fold increase in the frequency of T cells with a regulatory phenotype"
Abstract...."Consistent with the observed increase in Treg cell frequency, the CD25(hi) T-cell population was necessary for the suppressive activity of alemtuzumab-exposed T cells. The mechanism of this suppression was found to be dependent on both cell-cell contact and interleukin-2 consumption. These findings suggest that an alemtuzumab-mediated increase in the proportion of Treg cells may play a role in promoting the long-term efficacy of alemtuzumab in patients with multiple sclerosis".
So there we go dogma proved
Perhaps best data we have is from the CARE-MS I phase III trial
Freedman MS, Kaplan JM, Markovic-Plese S. Insights into the Mechanisms of the Therapeutic Efficacy of Alemtuzumab in Multiple Sclerosis. J Clin Cell Immunol. 2013 Jul 8;4(4).
"Tregs (i.e., CD4+CD25high), were significantly over-represented for the first 6 months after alemtuzumab treatment, even though the proportion of Tregs to total CD4+ T cells was similar in MS patients and healthy controls prior to treatment."
So after each infusion (at 0 and 12 months) the proportion of T regulatory cell number increases.
Don't believe it?
Why not look at the data...oh forgot you couldn't because Genzyme and the authors (including ProfG:-) have not published their findings despite reporting the work over 4 years ago!!!!.
There was no real mention in the pivotal trial data publications of anything except B cells are back to normal at 6 months and T cells are near normal after a year....Data not published, even in supplementary data!
Why not?
There was more in the ECTRIMS poster vault.
So there you have it every paper supports the concept that alemtuzumab selectively spares T regulatory cells and suggests that they increase after alemtuzumab.
This is why MS is inhibited. QED. I think this maybe right but not because of this data
So it all works great, if you think MS is a T cell issue, Treg cells outnumber the T cells, MS is stopped. However at 12 months after treatment they are back to normal and the T cells are still wiped out of existence for another 12 months or more. So when the T regs surge there are no pathogenic cells to regulate they are gone for a few years. So this idea doesn't hold much water
But what if there is a B cell problem?
then perhaps your ideas are up s**t creek without a paddle:-(
Now remember what I said above!
Base your assumptions on absolute numbers not percentages.
So back to Cox et al. 2005. Was there a balls-up?
So how many T regulatory cells are there?
Bonzoforgot (one of the readers LOL)...go get your calculator so we can work this one out:-). However, hope you can do the important bit without one.
If we look at Figure (above. It was 1A in the original) for total CD4 T cell numbers.
There are about 850-900 CD4 cells per microlitre at baseline (first point in graph above on the left ), So if there 3.7% CD4, CD25 T reg (according to the comment above) then there 3.7% of 850,000 cells/mL = 31,450 cells/mL.
So in Health about 30,000 T regs per millilitre (a thousandth of a litre of blood)
Now, if we look in the text in the Cox (pg 3335 in the paper) it says
"We attempted to demonstrate the functional ability of these cells....... ex vivo. However, we could not harvest sufficient cells; at 3 months after Campath-1H, 50 mL of blood from our patients..... yielded less than 100 CD4+CD25high cells.
So a maximum of 100 cells/50mL = 2cells/mL, 3 months after alemtuzumab:-(
Therefore after alemtuzumab we appear to go from 31,450 cells/mL down to 2 cells/mL, so hardly an amazing increase, as implied by the percentages (3.7% to 13.5%) and all the Treg supporting papers and in fact it represents over a 99.99% depletion.
The numbers are different but the percentages are consistent with the CARE MS I (findings below). However, I think the point is made, there it is a very, very significant decrease.
CARE-MS 1 data from EMA
This is what we found when we looked at the trial data results
Luckily in the phase III trial data the inferences are based on more
cells,
Therefore the implication of an increase is hardly relevant.
In my humble Opinion....The Question is Wrong.
It is not! What do T regs do, to control MS?
It is! What do Tregs do to control secondary autoimmune side effects of alemtuzumab in MS?...answer is nothing. They are not there to control secondary autoimmunity and that is why you get them. However they have returned before the pathogenic cells causing MS return therefore you have an induction therapy effect.
This latter question was thought about and dismissed
Joanne L. Jones, Chia-Ling Phuah, Amanda L. Cox, Sara A. Thompson, Maria Ban, Jacqueline Shawcross, Amie Walton, Stephen J. Sawcer, Alastair Compston, and Alasdair J. Coles. IL-21 drives secondary autoimmunity in patients with multiple sclerosis, following therapeutic lymphocyte depletion with alemtuzumab (Campath-1H)