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Pulmonary arterial hypertension (PAH) is an incurable disease associated with viral infections and connective tissue diseases. The relationship between inflammation and disease pathogenesis in these disorders remains poorly understood.
To determine whether immune dysregulation due to absent T cell populations directly contributes to the development of PAH.
Vascular endothelial growth factor receptor 2 (VEGFR2) blockade induced significant pulmonary endothelial apoptosis in T-cell deficient rats but not in immune-reconstituted (IR) rats. T cell-lymphopenia in association with VEGFR2 blockade resulted in periarteriolar inflammation with macrophages, and B cells even prior to vascular remodeling and elevated pulmonary pressures. IR prevented early inflammation and attenuated PAH development. IR with either CD8 T cells alone or with CD4-depleted spleen cells was ineffective in preventing PAH whereas CD4-depleting immunocompetent euthymic animals increased PAH susceptibility. IR with either CD4+CD25hi or CD4+CD25- T cell subsets prior to vascular injury attenuated the development of PAH. Immune reconstitution limited perivascular inflammation and endothelial apoptosis in rat lungs in association with increased FoxP3+-, IL-10- and TGF-β– expressing CD4 cells, and upregulation of pulmonary bone morphogenetic protein receptor type 2 (BMPR2)-expressing cells, a receptor that activates endothelial cell survival pathways.
PAH may arise when regulatory T cell (Treg) activity fails to control endothelial injury. These studies suggest that regulatory T cells normally function to limit vascular injury and may protect against the development of PAH.
PAH is a frequently lethal disease of relatively mysterious origins. For over 50 years it has been recognized that autoimmune phenomena are associated with certain forms of PAH, but it has never been previously demonstrated that autoimmunity, itself, may be a root cause for PAH 1. Previous work by our group and others demonstrated that T-cell immunity is involved in PAH pathogenesis, but no study has yet sought to explain how immune dysregulation directly causes PAH. Human and rat lung PAH pathology demonstrate occlusive arterioles and immune cell aggregates composed of macrophages, mast cells, B and T lymphocytes and anti-endothelial cell antibodies (AECAs) adherent to injured vasculature 1-4. Conditions commonly associated with PAH, such as systemic sclerosis and HIV, are associated with abnormalities in CD4 T cell function and exhibit a similarly inflamed pulmonary vascular pathology 1, 5. To date, it has not been clear whether inflammation surrounding the pulmonary vasculature is primarily the cause or the consequence of vascular remodeling. Given that athymic animals, which are congenitally T-cell deficient, are also particularly susceptible to the development of experimental PAH 6-8, we questioned whether inappropriately exuberant inflammation due to the lack of normal immune regulation could be a key predisposing factor for the development of this disease in these animals.
Injury resolution is an established function for a subset of T cells with strong regulatory activity, commonly referred to as Tregs. These cells typically express the co-receptor CD4+, the transcription factor Forkhead box protein 3 (FoxP3), and highly express the IL-2 receptor-α chain (i.e.CD25hi) 9. In addition to these classical Treg populations, rats also exhibit regulatory activity in CD4+CD25- cells10,11, 12. Tregs participate in the regulation of immune responses following a variety of inflammatory injuries such as burns and infection 13-15. In the absence of normal Treg activity, inflammatory injury is less readily resolved, and serious disease may develop 16.
Our group and others have demonstrated that the athymic rat develops severe PAH following vascular injury induced by monocrotaline (MCT) or VEGFR2 blockade (SU5416) 6-8. Compared to other PAH models, which require chronic hypoxia or a surgical pneumonectomy, T cell immunodeficiency renders these athymic animals particularly sensitive to the development of severe PAH under normoxic conditions. The athymic rat is the result of an autosomal recessive mutation on the rnu locus (rnu/rnu) of chromosome 10 leading to T-cell deficiency, thymic aplasia and hairlessness 17. Following MCT or SU5416 administration, athymic rats of different genetic backgrounds develop significant RV remodeling, perivascular inflammation and occlusive arteriolar lesions that are similar to lesion observed in severe clinical PAH 6-8. Prior studies utilizing athymic rats were limited by the availability of inbred animals which precluded an evaluation of how immune dysregulation could account for the PAH diathesis 7. In this study, we administered SU5416 to genetically-inbred athymic animals and performed immune reconstitution (IR) experiments with MHC-identical cells to assess, for the first time, the role of immune regulation in the development of PAH.
A detailed Methods can be found as an online supplement available at http://circres.ahajournals.org.
The experimental protocol was approved by the Veterans Affairs Palo Alto Animal Care and Use Committee. Inbred WAG (RT1u) ATHYMIC nude rats (rnu/rnu) and euthymic (rnu/+) rats were utilized for these studies (Biomedical Research Models, Inc, Worcester, MA). Euthymic rats served as MHC-identical controls and as cell donors for adoptive transfer experiments. Six to eight week old animals were injected s.c. with a single dose of either VEGFR2 antagonist SU5416 (20 mg/kg) dissolved in DMSO or DMSO (vehicle) alone. This dose was previously determined to be effective for inducing PAH in athymic rats 7. SU5416 was synthesized utilizing a previously described modified protocol 18. All animals were maintained in normoxic conditions.
20×106 unfractionated spleen cells obtained from euthymic male rats were injected into athymic rats i.p. 7d prior to SU5416 administration except for the time-course experiment in which they were injected at d-7, d-5, d-3, d0, d3, d5, d7 and d10, with d0 being the day of SU5416 administration. For CD4+ and CD8+ T cell reconstitutions 20 × 106 cells were administered i.v. to athymic rats, and for CD4+CD25hi and CD4+CD25- cell reconstitutions, approximately 3 × 106 cells were administered i.v. to athymic rats 7d prior to SU5416 administration.
Spleens from inbred euthymic rats were processed and filtered through a 100 μm cell strainer to obtain a single cell suspension, washed with DMEM, and then counted. CD4+ T cells were purified by labeling B cells, NK cells, CD8+ T cells, CD68+ cells, and mast cells with the following purified antibodies (all of which were mouse IgG1 isotype): anti-CD45RA (OX-33), anti-CD161a (10/78), anti-CD8a (OX8), anti-mast (AR32AA4) (all BDPharmingen), and anti-CD68 (ED-1) (AbD Serotec). The labeled splenocytes were then incubated with rat anti-mouse IgG1 microbeads (Miltenyi Biotec) according to the manufacturer's description. Live cells were recovered using the magnetic activated cell sorting (MACS) system with magnetic LS columns (Miltenyi Biotech). The collected negative fraction and enriched CD4+ T cells were further purified with a cell sorter (FACSAria) (BD Bioscience). The average purity was >98%. The same procedure was used to isolate CD8+ T cells except that instead of labeling the splenocytes with anti-CD8a prior to incubation with microbeads, they were labeled with purified anti-CD4 (OX-38) (BD Pharmingen) (average purity>98%). To obtain the CD4+ T cell depleted splenocytes, the splenocyte suspension was incubated with anti-CD4 (OX-38 and OX-35) antibodies (BD Pharmingen) and then the negative fraction was isolated with microbeads as described above.
Spleens were removed from inbred euthymic rats and prepared as a single cell suspension as described above. CD4+ T cells were purified as described above. To obtain CD4+CD25hi and CD4+CD25- subsets, pure CD4+ T cells were labeled with mouse anti-CD25-PE antibody (OX39) (BD Pharmingen) followed by incubation with anti-PE microbeads. LS columns (Miltenyi Biotec) were used with the MACS system to fractionate the two populations. Both cell fractions were then sorted with a fluorescent activated cell sorting machine, FACSAria (BD Biosciences). The average purity obtained was >97.5%. Expression of FoxP3 in both of these populations was assessed by using the FoxP3 staining set buffers (eBioscience) for intracellular staining with anti-FoxP3 antibody (150D) (Biolegend) according to the manufacturer's protocol. These cells were co-stained with antibodies to CD4 (OX-38), CD8a (OX8), CD25 (OX39), IL-10 (A5-4), CD45RA (OX-33) (all BD Pharmingen), and TCR (R73) (eBioscience). Flow cytometry was performed on a FACSCalibur (BD Biosciences) and the data was analyzed with CellQuest software (BD Biosciences).
The rats were anesthetized with ketamine hydrochloride (70 mg/kg) and xylazine (10 mg/kg) injected i.p. before right and left heart catheterization. Right ventricular systolic pressure (RVSP) measurements were obtained by insertion of a Micro Tip pressure transducer catheter (model SPR-671, 1.4F) (Millar Instruments) through the jugular vein into the RV. Signals were recorded continuously with a TC-510 pressure control unit (Millar Instruments) coupled to a Bridge Amp (AD Instruments). Data was collected with the Powerlab4/30 data acquisition system (AD Instruments) and analyzed with Chart Pro software (AD Instruments). LV combined pressure-volume signals were recorded by insertion of a pressure- volume conductance (PV) catheter (model SPR-838, 2F) (Millar Instruments) through the carotid artery into the LV. Subsequently, a median sternotomy was performed, the pericardium was opened and the PV catheter was introduced into the RV for measurements of RV pressure loops and pulmonary artery pressures. The PV catheter was connected to a MPVS Ultra single segment pressure volume system (Millar Instruments) and signals were recorded digitally. All data were acquired and analyzed with Chart Pro software (AD Instruments). The RV was dissected from the left ventricle (LV) and the septum (S) and each was weighed. The ratio of RV/(LV+S) was calculated to determine the degree of RVH.
GraphPad Prism® was used for statistical analysis. Differences between multiple groups were compared using one way ANOVA with Bonferonni multiple comparisons test for post hoc analyses. For datasets with non-parametric data, multiple groups were compared using the Kruskal-Wallis test and Dunn's multiple comparisons test was used for the post test analysis. For the cytokine, histologic and western blot analyses, unpaired T-tests assuming unequal variances were utilized with the comparisons being negative athymic control vs. athymic SU and athymic SU vs. athymic IR-SU groups. All data are represented as means ± SEM, and P-value < 0.05 is considered significant.
We first investigated whether inbred athymic rats exhibited more profound PAH than euthymic rats on a WAG strain (RT1u) genetic background. The heterozygous rnu/+ euthymic rats used in this study are T cell-replete and are MHC-identical to the athymic rats; a characteristic that makes them suitable as T cell donors for the athymic rat. Right ventricle systolic pressures (RSVPs) were used to estimate PAH. SU5416-treated athymic rats developed severe PAH and right ventricular hypertrophy (RVH) compared to immune-replete SU-5416-treated euthymic rats, and vehicle (DMSO)-treated athymic controls. To test whether IR with splenocytes from euthymic donors was protective against the development of PAH, athymic rats underwent IR with 20 × 106 spleen cells 7d prior to SU5416 administration; IR was later confirmed by flow cytometry of peripheral blood 7d after cell injection. IR prevented the development of PAH (Figures 1A, B). PAH was associated with histologically-evident pulmonary vascular remodeling which was prevented by IR (Online Figure I). IR led to a larger percentage of vessels being open compared to athymic SU5416 animals (Online Figure II). Additionally, pressure-volume studies were performed, the RVSP and dp/dt max data from these studies supported the hypothesis that athymic SU5416 animals develop significant PAH and that the PAH is minimal in IR-athymic SU5416 animals (Online Figure III; Online Tables I and II).
To confirm PAH by echocardiography, animals from the three athymic treatment groups were compared. SU5416-treated athymic rats had significantly faster pulmonary artery acceleration times (PAAT) (Fig. 1C), and an expanded pulmonary artery diameter (PADia) (Fig. 1D); parameters all indicative of worsening PAH. No significant echocardiographic left ventricle differences were noted between the three groups (data not shown). To address whether IR protection from PAH required that the reconstituted cells be present close to the time of SU5416-mediated vascular injury, athymic-SU5416-treated rats underwent IR at multiple time points relative to SU5416 administration and were evaluated at d21 (Figure 2). IR became progressively less effective the later it was performed relative to vascular injury. These results suggested that the protection conferred by IR involves controlling pathological events soon after the induction of vascular injury by SU5416.
To assess the possibility that regulating early inflammation was responsible for the protective effect of IR, animals were evaluated d7 after SU5416 administration. Inflammation with macrophages and B cells was pronounced by d7 (Figures 3A-D). Notably, PAH was not detected by right heart catheterization or echocardiography prior to 10d nor was there evidence of histological evidence of vascular remodeling at this early time points. To determine whether there was evidence of systemic inflammation, we next evaluated two key cytokines that have been previously implicated in the development of PAH: IL-6 and TNF-α 19, 20. Serum was obtained from animals 7 and 21d after SU5416 or vehicle treatment and evaluated by ELISA. PAH was associated with high serum IL-6 and TNF-α levels, and was suppressed by IR (Figure 3E, F).
Given that the systemic anti-inflammatory effect that IR had on SU5416-treated animals was detected within 7d of SU5416 administration, we next investigated whether anti-inflammatory Tregs could be detected in the lungs and blood of reconstituted animals at the time when the anti-inflammatory effect was noted. Putative Treg cells (CD4+CD25+FoxP3+; CD4+IL-10+) were readily detected in periarteriolar areas and peripheral blood of IR athymic rats 7 days after IR (Figure 4A-D; Online Figure V). Because TGF-β is an important cofactor expressed by Tregs to maintain self-tolerance following vascular injury 21, 22, we subsequently investigated the expression of TGF-β as well as phosphorylated Smad2 and Smad3 (pSmad2/3), which are cytosolic proteins involved in TGF-β signaling. Lungs of IR-athymic rats demonstrated CD4+TGFβ+pSmad2/3+ cells, and Western blot analysis confirmed increased pSmad2 levels in IR athymic animals (Figure 4E-I). This early accumulation of putative Treg cells expressing the anti-inflammatory cytokines, TGF-β and IL-10, correlated with the suppression of pulmonary and systemic inflammation (Figure 3) observed in reconstituted rats.
We next sought to determine which cellular subset of spleen cells used for IR was essential for the prevention of vascular injury and PAH. Although the athymic rat lacks T cells, it has a normal complement of bone-marrow-derived B cells. While T-dependent responses such as transplant rejection and hypersensitivity reactions are impaired in these rats, the innate immune response is intact, including mast cells, NK cells, macrophages and neutrophils 17. Therefore, the assumption was that a missing T cell subset (absent in athymic animals) was responsible for these rats’ predisposition for disease. We hypothesized that a putative CD4+ Treg population was the essential T cell subset. To rule out that CD8 T cells conferred protection against the development of PAH, we next immune-reconstituted animals with 20 × 106 fractionated CD8+ T cells 7d prior to SU5416 administration and assessed the rats at d21. IR was confirmed by flow cytometry of blood at 7d post SU5416. CD8+ T cell reconstitution was non-protective (Figures 5A, B). Next, to rule out the possibility that other spleen cell populations besides CD4+ T cells were conferring protection, IR was performed with CD4-depleted spleen cells. As with CD8+ T cell reconstitutions, depletion of CD4+ cells from the spleen cell inoculums prior to IR, eliminated the ability of adoptively transferred splenocytes to block PAH and further confirmed that the protective subset of cells was CD4+ (Figures 5C, D).
While we established that it is possible to uniquely generate PAH in rats under normoxic conditions that have a genetic absence of T cells, we thought that the relevance of the general model would be strengthened if an immunologically normal rat exposed to simultaneous vascular injury and CD4 depletion would also develop PAH; the immune system of animals devoid of all T cells from birth may develop in unconsidered ways. For this reason, we investigated, immunologically-intact euthymic rats, which are normally refractory to developing significant PAH with SU5416 therapy in normoxic conditions (Figure 1). Administration of a CD4-depleting monoclonal antibody, which eliminated >98% of circulating CD4+ T cells prior to SU5416 administration, rendered these animals susceptible to the development of PAH (Figure 5E, F; Online Figure V). CD4-depleted animals developing PAH demonstrated increased perivascular inflammation with macrophages and B cells (Online Figure VA, B). These studies cumulatively demonstrated that a population of CD4+ T cells was required to prevent PAH.
To determine if CD4+ cell subsets were differentially protective, athymic rats were reconstituted with either CD4+CD25hi cells or CD4+CD25- cells. Cell subset purity following isolation was ≈98%. CD4+CD25+FoxP3+ cells were detected in the blood 21 days after SU5416 (Online Figure VII) in both CD4+CD25hi-reconstituted athymic rats (4.8% of circulating CD4+ cells) and CD4+CD25--reconstituted animals (1.5% of circulating CD4+ cells); the latter finding being consistent with a peripheral conversion of CD4+CD25- cells into CD4+CD25+ cells 23. Both CD4 T cell subsets attenuated the development of PAH (Figures 5G, H). Therefore, in this rat model, both CD4+CD25hi cells and CD4+CD25- cells exhibited regulatory activity.
Because PAH induced by SU5416 has been attributed to the death (by apoptosis) of vascular endothelial cells 24, we evaluated whether IR also attenuated this process. The presence of apoptotic cleaved caspase 3+ CD31+ cells was first noted in SU5416-treated animals 7d after SU5416 administration (Figure 6A). Vascular apoptotic cells was more marked by d21 when CD31 staining is minimal presumably due to prior endothelial cell death (Figure 6B). In established PAH, apoptotic cells within the vascular wall were notably CD31-. Evidence of widespread pulmonary apoptosis was also demonstrated by increased lung cleaved caspase 3 protein levels in non-reconstituted SU5416 animals on day 7 (Figure 6C, D) and 21 (Figure 6E, F). A morphometric assessment of cleaved caspase 3+ cells/per vessel demonstrated relatively fewer apoptotic cells/vessel in IR-athymic rats (Figure 6G).
To further evaluate why IR was protective against endothelial apoptosis, we next investigated BMPR2 levels in the three treatment groups. Given that BMPR2 is a protein characterized as vascular-protective in health and vascular-defective in PAH25, we tested whether IR impacted the expression of this receptor in lung tissue. Notably, all three groups exhibited rare BMPR2-expressing macrophages (Figure 7A). Global lung tissue BMPR2 levels appeared elevated in athymic IR-SU by immunochemistry (Figure 7B). BMPR2-expressing cells were frequently noted adjacent to CD4+ cells in immune reconstituted animals (Figure 7C). Vascular BMPR2 expression in athymic IR-SU was notably elevated (Figure 7D, E). By Western blot analysis of whole lysates, BMPR2 expression was significantly increased in athymic IR-SU animals (Figure 7F, G). Thus, the protection conferred by immune reconstitution in this PAH model was strongly associated with upregulation of pulmonary BMPR2.
The observation that T cell-deficient athymic rats develop particularly exaggerated PAH 6-8 and that immunodeficiency itself promotes autoimmunity 26 suggested that restoring a missing lymphocyte population could prevent PAH by limiting inflammation. Here we demonstrate for the first time that IR attenuates early inflammation following vascular injury induced with a VEGFR2 inhibitor and is protective against the subsequent development of PAH. IR of athymic animals was only effective if administered prior to SU5416 administration. This finding is consistent with the idea that in normal, immunocompetent animals, the early promotion of injury resolution by Tregs suppresses vascular inflammation and prevents PAH. In PAH development in the SU5416 model, ongoing pulmonary vascular endothelial injury and apoptosis is followed by a progressive proliferative phase of phenotypically abnormal luminal cells; coupled with vascular smooth muscle hypertrophy and vasoconstriction, these pathological changes significantly increase the pulmonary vascular resistance and cause PAH 27. This process is modeled in Figure 8.
Inflammation in T-cell deficient animals was notable for an accumulation of B cells and macrophages within one week of SU5416 administration. This finding is concordant with the fact that the loss of self-tolerance in animals missing normal Treg populations is associated with the appearance of various autoantibodies and autoimmune disease 28, 29. With complete elimination of CD4+CD25hi cells, systemic autoimmunity occurs as manifested by multiorgan inflammation and autoantibody production 16. Thus a loss of Treg-mediated self tolerance leads not only to a loss of T cell tolerance but also to a breakdown in B cell tolerance. Moreover, recent data demonstrate that regulatory T cells are not restricted to regulation of the adaptive immune system but also affect the activation and function of innate immune cells including monocytes, macrophages, dendritic cells and NK cells 30, 31, 32, 33. Exuberant inflammation following vascular injury in our model can therefore be explained by a loss of self-tolerance in the absence of normal immune regulation. We determined that both CD4+CD25hi and CD4+CD25- populations were sufficient for IR-mediated protection from PAH. While CD4+CD25hi are well described as the Tregs in mice, rats exhibit additional Treg populations compared to mice. In rats, coexpression of CD25 on CD4 T cells does not consistently identify all CD4 cells with regulatory function 10. Several studies10-12 demonstrate regulatory activity in the CD4+CD25- population in rats, and this population also appears to have regulatory activity in the current model. We also present evidence that immune reconstituted CD4+CD25- cells may have been converted to CD4+CD25+ Tregs as has been previously described 23. Whether it is this conversion in the periphery or the fundamental nature of rat CD4+CD25- subset, these cells clearly demonstrated regulatory activity. The identification of Tregs as a crucial component of self-tolerance in other diseases has led to major advances in the understanding of how immune injury in autoimmunity and transplantation can be initiated when either insufficient numbers of Tregs or compromised Treg function occurs 34, 35.
TNF-α and IL-6 were elevated in the serum of rats developing PAH. TNF-α over-expression augments PAH19. IL-6, a pro-inflammatory and vasodepressor cytokine, has been shown to have a significant association with mortality in patients with PAH 36. Increased serum and plexiform lesion levels of IL-6 have been found in PAH patients as well as in IL-6 Tg+ mice with replicative pathophysiological changes of PAH 37. IL-6 has also recently been found to negatively regulate the TGF-β/BMP signaling cascade 38. The current study demonstrates that Tregs limit the systemic liberation of IL-6 and TNF-α, a finding that lends credence to the concept that Tregs have therapeutic potential in immune-mediated inflammatory diseases characterized by high levels of these cytokines 39, 40.
While prior studies have described TGF-β in relation to the vascular endothelium in PAH (e.g. 41;), the current study highlights how active TGF-β may also be an important cofactor expressed by Tregs to maintain self-tolerance following vascular injury 21, 22. The proposed mechanisms by which Tregs control inflammation are numerous and involve several basic mechanisms including: 1) secretion of anti-inflammatory cytokines (most notably TGF-β and IL-10), 2) cytolysis of effector T cells, 3) metabolic disruption of effector cells (for example, by serving as an IL-2 ‘sink’ due to high Treg surface concentrations of the IL-2 receptor protein) and 4) modification of dendritic cell function (such as through the induction of the immunosuppressive enzyme indoleamine 2,3-dioxygenase) 42. A striking accumulation of putative Tregs on day 7, including CD4+FoxP3+ and CD4+TGFβ+pSMAD2/3+, CD4+IL-10+cells, were noted in only the IRSU5416 lungs and were concentrated around the arterioles. Whole lung lysate levels of pSMAD2 levels were evaluated and were increased in the IR group on d7. Over time, the diseased athymic-SU5416-treated animals developed increasing pSmad2 levels as well, indicating that increased TGFβ signaling, in isolation, can't explain protection from disease but should be considered in the context of which cells are involved. Tregs noted around the pulmonary arterioles in IR animals also expressed IL-10. IL-10–mediated Treg effects have been particularly evident in antigen-specific responses and represent a normal compensatory mechanism antagonizing the inflammatory response 43, 44. IL-10 is a potent immunomodulator that inhibits the secretion of various proinflammatory cytokines, including IL-6 and IL-8. Adenoviral expression of IL-10 protects against monocrotaline-induced pulmonary hypertension in rats 45. Thus, IL-10 and TGF-β expression by Tregs offer plausible mechanisms explaining how these cells limit inflammatory injury and possibly accelerate pulmonary recovery.
IR resulted in decreased vascular apoptosis following SU5416 administration. Because endothelial apoptosis is the chief mechanism by which SU5416 induces PAH 46, we sought factors associated with IR which could have protected endothelium and found that IR induced vascular BMPR2 expression. BMPR2 mutations are strongly associated with familial PAH 47, and decreased pulmonary vascular BMPR2 expression is associated with idiopathic PAH 48. In experimental models, hypoxia-induced PAH is associated with down-regulation of pulmonary vascular BMPR2, and genetic ablation of pulmonary vascular BMPR2 favors PAH development 25. In the current study, BMPR2-expressing cells in athymic control and athymic SU5416 groups were confined to rare cells that we were not able to characterize except that they were sometimes CD68+ macrophages. By contrast, IR athymic SU5416 animals exhibited large numbers of BMPR2-expressing cells often adjacent to CD4+ cells. Additionally, we demonstrate increased BMPR2-expressing pulmonary vascular cells only in the IR group. The mechanism by which IR could result in such BMPR2 upregulation is not known, nor is it understood if there is a direct causal relationship between immune competency and BMPR2 expression. Of interest, a close (physical) association between BMPR2 expressing cells and T cells was recently observed in idiopathic PAH 49, and future studies will investigate by what mechanism T cells might directly induce endothelial BMPR2.
Treg IR studies in rats are costly, time-consuming, and have limited reagents available compared to mice, but rat models benefit from more robust disease that more closely resembles human PAH pathology 50. While pulmonary inflammation in PAH is a well-established phenomenon 3, 5, it has been unclear whether the inflammation is itself pathogenic or is a secondary immune response to preexisting pulmonary vascular disease. The current study strongly implicates inflammation associated with CD4 immunodeficiency as a primary predisposing factor to experimental PAH development. The clinical relevance of this finding is that certain PAH-associated conditions are characterized by abnormalities in CD4+ T cell number and function. Examples of this association include HIV infection and autoimmune diseases such as systemic sclerosis, systemic lupus erythematosus, polymyositis, Hashimoto's thyroiditis, Sjögren's Syndrome and the antiphospholipid antibody syndrome51-57. The clinical relevance of this issue is that these CD4+ T cell irregularities may render patients susceptible to exaggerated vascular inflammation and subsequent vascular remodeling following vascular injury. By distinction, idiopathic PAH has been characterized by increased Tregs in peripheral blood accompanied by a four-fold elevation of lung CD8+ cells 58, 59. Therefore, in the case of idiopathic PAH, if immune dysregulation contributes to the lung inflammation observed in this condition, current evidence does not link pulmonary injury to abnormal CD4+ T cell populations detectable in the periphery. Correcting immune dysregulation with Treg therapy 60 is an exciting application in development which could prove useful for some PAH conditions 60. Greater recognition that PAH patients have a condition that may begin with impaired resolution of vascular injury could have a significant impact on how this condition is both understood and treated.
What is Known?
What New Information Does This Article Contribute?
Clinical conditions commonly associated with PAH, such as systemic sclerosis and HIV infection, are characterized by abnormal CD4 T lymphocyte function and number - T cell abnormalities that are likely responsible for some of the dysregulated immunity observed in these conditions. Pre-clinical studies have shown that T-cell deficient rats develop lung inflammation and exaggerated PAH following vascular injury. The purpose of the current study was to determine whether restoring T lymphocyte function and number abrogates exuberant inflammatory responses and preventes PAH. We found that lung injury resolution, in the presence of Tregs, is associated with significantly less inflammation and endothelial apoptosis. Inflammation was not merely a consequence of PAH because inflammation and apoptotic cell death occurred prior to the development of vascular remodeling and elevated pulmonary artery pressures. Unexpectedly, the restoration of T cells also led to upregulated vascular BMPR2 in protected rats. This finding is of interest because BMPR2 mutations have been implicated as a cause of familial PAH, and decreased pulmonary vascular BMPR2 expression has been observed in other forms of PAH. These findings suggest that anti-inflammatory Tregs, in association with inducible BMPR2, provide innate protection against PAH following pulmonary vascular injury.
The authors thank Dr. Marty Zamora and Dr. Joshua Beilke for critically reading the manuscript.
SOURCES OF FUNDING
This study was supported by NIH grant HL082662 to M.R. Nicolls and the Stanford NHLBI Proteomics Center NHLBI-HV-10-05.
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