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tagline 1999

Gladstone Immunologist Challenges Thymic Status Quo, Teasing the Research Forward


'Problem of production'

In HIV infection, the role of the thymus remains both hotly disputed and poorly understood -- whether its role in leading to the clinical manifestations of disease or in rebuilding an already HIV-ravaged immune system. Along with a handful of other pioneers in this work, Joseph "Mike" McCune has been at the forefront of immunological research for over a decade. TAGline checked in with him this summer for an update of his most recent research and for a hint of where we might be headed -- or need to go.

It seems like we know more now about the thymus in HIV infection than we know about the bone marrow. Am I wrong?

I would say that they are both understudied. It has been known since the mid-1980s that the bone marrow is infected by HIV. So even before we had, say, AZT trashing red cells many people came in with bone marrow abnormalities. This has been well documented -- but not very vigorously pursued. It's a difficult thing to do.

For obvious reasons, I guess. But if the source of T cells is actually the bone marrow -- with the thymus serving only as the "boot camp" or "finishing school" for the progenitor cells which emerge from the bone marrow's stem cells -- would correcting the pathology in the thymus not matter as much if the migrating cells from the bone marrow are already not fully functional?

That's right. If, for example, you had a fully functional thymus but no bone marrow, it wouldn't help. It'd be like having a car without gas.

Let's talk briefly about the work you presented at the Lago Maggiore resistance workshop last summer and which was published last June in JCI [Journal of Clinical Investigation]. Basically you showed what you called "abundant thymic mass" in about 50% of the HIV-infected adults you looked at. Many over age 40 had it, and in people younger than 40 with CD4 T cell counts between 300-500, a whopping 93% of them showed evidence of thymic mass (on CT scans). Did anything about that research surprise you?

Oh yeh! The reason that we knew more about the bone marrow than the thymus until that study is that, up until that time, [it was widely assumed that] the thymus would not be present at all in adults.

Yeh, that was the prevailing ... Mark Harrington called it the "hoariest dogma" of immunology.

We had actually studied, using these chimeric mice, in the early 1990s ... we spent a lot of energy studying ... how HIV can destroy the thymus. And it does so because it infects CD4 positive cells, which are key cells. So we had those data, and there were data in SIV-infected monkeys that the thymus is destroyed, and there were data in HIV-infected babies that the thymus is destroyed. So when it came to adults, the "hoariest dogma" said that the thymus would be much smaller -- if it was there at all. And if HIV was around, then it was most certainly not going to be there because HIV destroys the thymus, right?

Our study was set up, actually, to understand whether or not the hoariest dogma was true -- because it had not yet been studied in HIV-infected adults. And what that paper showed, basically, was that by relatively crude measures (CT scanning and analysis of these so-called "naive T cells" by phenotyping in the peripheral blood) that there does appear to be thymic mass and function in HIV-infected adults. That was surprise number one. And surprise number two was that it's even easier to find evidence of thymic tissue and function in HIV-infected compared to age-matched HIV-uninfected adults.

Yeh, I didn't catch that in your Lago Maggiore presentation, but when I read your JCI paper last night, that's really amazing.

Yeh, we were surprised by that. Of course there is still a fair degree of uncertainty about whether what we're looking at is truly functional thymus. (CT scanning is not capable of distinguishing between thymic tissue and tissue that might simply be a conglomeration of inflammatory or malignant cells.) We know now, however, that it is possible to look at other surrogates of thymic function, such as TREC (deletion circles) as have been studied by Danny Douek in Rick Koup's lab, by Sharon Lewin in David Ho's lab, and by Jean-François Poulin working with Rafick Sekaly and myself. Study of these surrogates also suggests that thymic function is present in adults, even some of those who are HIV-infected.

So they sort of corroborate each other.

Yes. I think the datasets that are coming back now all seem to be consistent with one another. Which is to say that the thymus is functional in many adults; that the function decreases as people get older; and, most importantly, that there is a tremendous amount of heterogeneity amongst HIV-infected adults: some have abundant thymus and others have little apparent thymic function. So, when considering the effects of HIV and treatment in adults, an important variable might be whether the individual has thymic function or not.

And there's really no way to predict this based on age, viral load, CD4 cell count or duration of HIV infection. Is that right?

Partly. We did notice that more abundant thymic tissue was present in young, HIV-infected adults and, amongst those, especially in individuals with falling CD4+ T cell counts, between 300-500. As you mentioned, over 93% of such individuals having abundant thymic tissue, which is extraordinarily high.

So do you think the thymus "realizes" that something is going on and so it revs itself up and tries to compensate for the destruction or disappearance of these T cells -- and then at some point either HIV gets the best of it or it just can't keep up?

Good, yeh. So the working hypothesis is, as you say, that there is compensatory positive feedback on the thymus -- and maybe also on the bone marrow when T cells are depleted in the periphery. And as long as the thymus can compensate (by making more cells), then the immune system in the periphery will not collapse -- because you'll just make more cells. Now ... we may as well talk about it now, because this is where the "tap" and "drain" debate comes in. The tap is now the thymus: it's producing more cells. And when the "drain" is open, more cells are made in order to compensate for the fact that the "sink" is emptying faster, okay?

Now David Ho, when he first postulated tap/drain, talked about exhaustion. The tap became exhausted. Right? And could no longer compensate, if you will. But "exhaustion" needs to be defined biologically; cells don't "get tired." If they do, there's something called senescence... after a certain number of divisions...

Yeh, that was the telomere paper.

Telomeres, right. Yes, it's possible that they might get so old -- that they've divided so many times -- that they can divide no more. That's one physical correlate of exhaustion. Another correlate, which I think is supported more squarely by the data, is death. You know, "What would die?" Well, the tap would die. We know, as I mentioned, that HIV infects the thymus and kills the cells that are in it. Now, if the thymus is uninfected, it can work. Yet eventually, it would appear to us, that HIV is going to get sort of homogenized throughout the body. And it stands to reason even though there's a thymic-blood barrier in much the same way that there's a blood-brain barrier that the thymus is going to get infected by HIV. And once the thymus is infected by HIV, all bets are off. This compensatory increased production is not going to happen. And therefore the system is going to have destruction in the periphery and no production coming out to sustain the loss of cell.

This in fact is why in the Nature Medicine paper on production we state, my colleague Marc Hellerstein and I, that the disease is more a problem of production. That is to say, you can have the virus, but as long as the production systems are working there is no problem. But as soon as the production systems are hit, then you have a disease -- because the T cells go away and are no longer replaced.

And you're not alone. Fauci, Pantaleo, Miedema all seem to be advocating for an increased emphasis on the systems of production -- or "tap."

We're all still learning. We talk a lot about this. My scientific background has led me to work on the heterogeneous populations of blood cells that are found in the body. To me, it's part of my background to think about different types of cells and how they might be affected differently by HIV. Both "sides" in the debate are right -- some of us are simply pointing out that it's important to understand HIV's effects on progenitor cells as well as to think about the destruction of more mature cells.

So HIV's attacking the immune system from both ends?

Right. Now, there are several instances in which that doesn't happen with a lentiretrovirus, and these are very cool. One is in SIV. SIV infects a rhesus macaque, and causes basically AIDS. The T cells in the periphery go away, the animal gets sick and dies. The same virus, SIV, infects sooty mangabeys (another nonhuman primate) and what happens is NOTHING! The virus can go into the CD4 cells and kill the CD4 cells in the sooty mangabey, but the CD4 count goes down only slowly -- if at all. And one possibility, which is being pursued by a number of labs now, is that in this instance the virus has figured out how to kill mature cells but not how to kill the progenitor cells. And in this setting, actually, sooty mangabeys serve as a host for SIV in which the virus lives happily. So it's not a pathogen-as it is in the rhesus macaque -- it's a sort of a part of the ecosystem, instead.

So does that mean that the stem cells of these animals are naturally resistant to SIV -- and that we must wait for the day when gene therapy research has succeeded in its attempts to develop HIV-resistant progenitor cells?

Well, maybe it's that they're resistant but another possibility is that there are different types of HIV or, in this case, SIV. And that some are tropic more for progenitor cells than for mature cells and vice versa. So yeh, either possibility is right. A few, like Mark Feinberg, are working on this -- and Bob Grant.

But the other thing that's arisen, which I'm sure you're aware of is in HIV-infected adults who are "failing" therapy with high viral loads but who have viruses that are associated with rising CD4 counts. Now how the hell does that happen? This looks exactly like the SIV-infected mangabey to me! You have a virus which is present but it doesn't appear to be causing depletion of T cells the way the virus used to do. Cheryl Stoddart in my group has been studying viruses from such individuals with François Clavel. In Chicago in February they reported these viruses don't infect and kill the thymus.

So our working hypothesis is that in these individuals who have this virus/CD4 "disconnect," we're dealing with viruses that can kill CD4 cells in the periphery but which don't affect the systems of production (like, for instance, the thymus) as efficiently as they used to do. So the system can continue to make cells and pour them into the periphery even though there are lots of cells being destroyed there. Here, in other words, the "tap" is not getting tired.

Then, the hypothesis is that, what, there's something about one of these classes of drugs or the use of several classes in combination that restricts HIV to gnawing away only at the peripheral end of the T cells and prevents it from being able to affect production as much?

Hypothesis. That's the hypothesis behind the paper presented by Dr. Stoddart in Chicago. What was done there was based on work with a molecularly-cloned virus called NL43 (a CXCR4-utilizing synctia-inducing virus which we've used a lot). Put into these SCID-hu mice, this virus replicates quickly and destroys the thymus. François Clavel replaced the gag region of NL43 with gag that came from mutated regions of the protease gene of patients who had been treated and who had become resistant to either ritonavir or saquinavir. So we now had two viruses: one that was wild type NL43; the other was recombinant virus that included gag and protease regions from these patients that were resistant. The first virus went in and killed the thymus. The second virus went in and replicated slowly but didn't cause any cytopathicity in the thymus.

Wow.

The only difference was the insertion of these regions.

So we can make protease resistant virus work for us?

Well, maybe. I mean, who knows?

Is there any degree of confidence that these beneficial mutations would remain stable, though, over time?

No, we don't . We have no ... I mean this is an area which is being newly investigated.

Very exciting, though. I missed that in Chicago.

I think a lot of people were surprised by this finding when Cheryl gave the talk. We certainly were, too. And we're now very eagerly doing more studies on it. In general, I think the idea would be that virus from these HIV-infected individuals may have "evolved" to approximate the situation of SIV in the sooty mangabey -- that of a pathogen which can co-exist relatively well within the host.

In nature, most microbial agents live in harmony with their host. In the situation of SIV with sooty mangabeys, you have a case of a lentiretrovirus that can be a pathogen which lives relatively well with that host. It's an important question to understand why and if that can happen with HIV. We're trying to approach it from the angle of differential pathogenicity to the systems of production.

I need to bring this around to treatment research agenda and therapeutic applications at some point. And I was wondering, I guess there were two papers in Geneva on thymus transplants and I actually, I had remembered, maybe there were two or three, that they all pretty much were failures but then I saw in Brenda's report for HIV-Plus that the people who were more immune compromised did not reject the transplants.

Yes, I know those data are coming out.

I just wonder that if maybe with all the data that your group and Koup and Sharon Lewis at Aaron Diamond ... is research into thymic transplant less urgent now? Or is it possible that it won't even be necessary if we have these demonstrations of the thymus being active?

The way I look at it is this. Let's say we have an assay for thymic function that everyone agrees is good -- we don't have that yet, but let's say we do. I would imagine we'd apply that assay to HIV-infected people when they present to ask the question, "Do they or don't they have a thymus?" And we'll have two groups: one will have demonstrable thymic function and one won't. Okay? And of those that do, some of them will have, you know, rip-roaring function and the others will be left with only a trickle of production.

Okay.

Now, I'd guess that those who don't have thymic function will need to be treated differently than those who do. For instance, individuals in both groups may end up with an increased T cell count after therapy, but if the T cells do not arise from the thymus, they may not have a diverse T cell receptor repertoire. If so, these patients may still be prone to the problems associated with immunodeficiency. In other words, an increased CD4 count after HAART without a diverse T cell receptor repertoire may not be much help. So, in this scenario, we need to think about why they don't have a thymus. We've already noticed people who have increased their T cell counts post-therapy

Naive cells?

No, just their memory cells, actually. They get therapy. Their CD4 count goes up, and they end up having or getting still things like CMV retinitis. So an increased CD4 count after HAART without a diverse T cell receptor repertoire may not be much help.

But that's not what we're seeing clinically -- for the most part. Pretty much across the board we're seeing surprisingly competent immune reconstitution -- even if these new T cells are not emerging from the thymus. How do we square this "no diverse repertoire" theory with the current clinical reality?

In general, we are indeed seeing a decreased incidence of opportunistic infections in patients who are effectively suppressed on HAART. Immunologic studies (e.g., those done by Krishna Komanduri in my lab and reported last year in Nature Medicine) indicate that such reconstitution is associated with increased T cell responses against these pathogens (e.g., CMV). Presumably, these T cells are present before HAART was initiated (i.e., they didn't come recently from the thymus) and are able to respond to the pathogens once HIV is suppressed. But this is by no means the rule, however: Krishna, working with Judith Feinberg (U Cincinnati) and Jay Lalezari (San Francisco), has noted that some HAART-treated patients have CD4 T cell increases and yet continue to have CMV retinitis; these patients, of note, lack anti-CMV T cell responses.

We worry that these patients may be the ones who lack a diverse TCR repertoire (and possibly a thymus) and that they represent the tip of a larger iceberg. More ominously, we are concerned about the implications of these observations in the context of long-term survival post-HAART: those individuals without a diverse TCR repertoire may be unable to effectively combat new antigenic exposures in the future, e.g., from other infectious agents, malignant cells, and the like.

So we should expect a new gay malignancy epidemic down the road. Great. But why might some individuals still have functioning thymic tissue and others not-and how could we address this therapeutcially?

I see two possibilities. One is that these individuals lack the feedback mechanisms that turn the thymus on. Another is that they lack the thymus upon which that the feedback mechanisms might operate. So let's take those in order: If they lack the feedback mechanisms, then provision of the feedback mechanisms might be sufficient.

Which are?

Well, we don't know yet. That's what we're trying to figure out. But by analogy, erythropoetin causes more red cells to be made in the bone marrow okay? It's made in the kidney. People that have bad kidney disease have anemia. You know why? Because they don't make EPO.

Okay.

And the way you treat that is not to give them a bone marrow transplant. The way to treat that is to give them EPO.

So we have to find the "EPO" for the thymus?

There you go. First, though, we have to understand whether feedback on T cell production in the thymus can occur, as it does in the example of EPO. If there is such feedback, then we have to understand how it operates. That, in my mind, is an extremely important area of research -- precisely because of the potential therapeutic implications.

So we don't even know if there is, in fact, feedback?

No. In fact, everybody thinks there's not. First there's not a thymus, okay, that's one dogma. The other dogma is that the thymus is a little homunculus that does what it does on its own and then dies. So that's the second hoariest dogma... Since 1960 or so... There have been a lot of experiments -- most of them in rodents -- done on this. I mean lots -- to ask the question, "Is there feedback?" and the answer is "No," that "there's not." But I'm not convinced yet that this is right in the setting of HIV-infected adults.

So then, to continue, if we find out there's not a feedback problem, there are going to be some people who lack thymus. Now, in the thymus there are several things that they might lack. One thing they might lack is the progenitor cell that makes the thymocytes. In such people, for instance, the bone marrow might be trashed, and the thymus doesn't have any of these cells upon which feedback could operate. In these people maybe a bone marrow transplant would help. Because you could give them new stem cells that would then give rise to new progenitors that would go to the thymus, and feedback could work on those progenitors and you would make more T cells for the periphery.

Finally, of those who don't have a thymus there could be some who lack what's called "thymic epithelial tissue," the collection of cells which define the structure of the organ. And that, actually, is what's being transplanted now. For such people, maybe we could figure out how to do transplant of thymic epithelia tissue in a way that works-in much the same way that we provide transplants of kidney or liver. Alright? I guess my basic point is that I don't think all HIV-infected adults with poor thymic function will have the same underlying lesion. Once we have better definitions for thymic function, we'll find that patients will fall into subgroups and that the subgroups will require different therapies.

One quick question: extrathymic maturation of T cells.

Good!

Mario Roederer [Stanford University] has concerns that new naive T cells that mature outside the thymus do not have the diversity and function of new naive cells that come from the actual thymus. Is that your feeling?

That is the prevailing wisdom. Probably right. The situation for instance with di George syndrome (where there is no thymus) indicates that cells made extrathymically are not diverse. There are elegant studies done in frogs and birds by Max Cooper which indicate that if you remove the thymus early in life (like in utero), T cells are not made later. That is, there is no other source of T cell maturation. It's possible, though, that extrathymic T cell maturation could occur in settings of unusual stress. A number of labs (including ours) are asking that question. You know, biology is incredible in its ways of coping, right?

In the hematopoetic system, for instance, the bone marrow is normally the place in you and me -- adults, that is -- where these multilineage stem cells reside, okay? But if the bone marrow gets trashed-by radiation or chemicals or disease -- other organs that usually do not operate to be hematopoetic organs can turn on as hematopoetic organs -- including the liver, the spleen, even the thymus. This is called extra medullary hematopoesis. ("Medullary" stands for the bone marrow.) So, in settings of stress, EMH clearly occurs.

So what a number of us are asking is if, in situations of stress on the T cell system, if extrathymic T-poesis might occur. Most of the experimental models that have been analyzed to date are not stressed. Okay? So the patient in di George is cuddled. Little baby, right? Kept out of the way of harm. The frog and the bird that were studied in utero? Not stressed. So there remains the possibility that in certain pathologic situations extrathymic maturation might occur in a way that provides a diverse repertoire. But, to date, it's not been clearly shown.

May I ask one last question? People are talking about the potential for hGH, bringing back thymosin alpha, thymopentin. Do you think any of these might have a role?

Sure. Here's why. It's possible that these represent part of, or a adjunct to, whatever this feedback loop on the thymus are.

And one of these might be the thymic "EPO" we're looking for?

Maybe. We don't know. There's certainly suggestive data that cortisol, for instance, is a steroid hormone which is bad for the thymus. It causes the thymus to involute. Testosterone does the same thing.

And interferon-alpha?

In the mouse interferon-alpha appears to be a potent negative regulator of thymopoesis.

Okay.

And there are, in the literature, indications that other factors might actually promote thymopoesis. Growth hormone is one of those. IGF-1 (insulin growth factor), a mediator of growth hormone, is another.

These are in vitro data?

Most work has been done in vitro, but there are some anecdotal data in people as well. Patients who have acromegaly, for instance -- who have too much growth hormone -- can have big thymuses. It's all sort of still at the level of anecdote. And there are not very many -- if any, in fact -- good studies in humans because, you know, remember [he says wryly] "the thymus is not present in adults"; even if it's present, "it's not regulated." Right? So as a consequence of these prevailing "wisdoms," there have not been many studies to evaluate these questions about thymic hormones or other hormones which might act on the thymus. But there's more and more interest in this area now, and I think it's well worth the time to evaluate it. Because it would be attractive to be able to use commercially available products to promote thymopoesis.

And if people become more focused on the tap than they are currently on the drain, are the therapeutic implications significantly different?

Yes. Because if you're focused only the drain, you're mainly trying to figure out how to make a plug.

Which is ... antiretroviral therapy?

The plug in the case of the drain is antiviral therapy, right? If you're also thinking about the tap, then you might think of ways of making the tap work better, right?

Which would get us back to the thymic factors and the "EPO" for the thymus?

Or ... which promote production better. There might also be particular types of viruses that are especially cytopathic towards the progenitor cells. And there might be some drugs that work better against those viruses than against others. This is highly speculative, for HIV, but it's not at all for most other viruses. There is no such thing as another virus that has only one type, okay? There are some types of influenza viruses that are associated with clinically severe disease and others that are not.

Human papilloma virus (HPV), right? The virus that causes warts? In 1915 there were eighty different subtypes of HPV identified; some caused just warts and some caused cervical cancer. So it seems to me to be not outside the realm of possibility that there might be different subtypes of HIV -- not just X4 vs. R5 or SI vs. NSI -- but subtypes that have tropisms that are particular for stem cells or other progenitor cells. If so, there might be selective treatments that could be aimed at them. In other words, by focusing on the systems of production, we might also arrive at different ways of thinking about selective virus killing -- and ways to stop it.

Thanks Mike. A pleasure as always.