RECENT PROGRESS IN WELL DESCRIBED MODELS OF AUTOIMMUNE HEMOLYTIC ANEMIA
New Zealand black mice
Summary of previous findings
One of the initial models of AIHA, New Zealand black (NZB) mice spontaneously develop RBC autoantibodies that lead to hemolytic anemia by 6 months of age [8,9]. The NZB model has been instrumental in demonstrating that genetic factors contribute to the development of AIHA [10,11]. Multiple susceptibility and suppression genes (e.g., Aia1, Aia2, Aem1) have been identified and correlated with antierythrocyte autoantibody production [12,13]. Moreover, this model has demonstrated a role for MHC alleles in the predisposition to develop AIHA; NZB mice (which normally express MHC H-2d) that have been genetically modified to express MHC H-2b exhibit delayed onset of AIHA with lower autoantibody titers [14,15]. Additional analysis has revealed more risk factors for AIHA onset, including a shift in cytokine production, dysregulation of B and/or T lymphocytes, and pathogenic infections . Studies in the NZB model have also led to the identification of common RBC autoantibody targets (e.g., Band 3, Band 4.1) and allowed for autoantibody cloning, which, in turn, allowed for mechanistic analysis of the relationship between autoantibody subtype and RBC hemolysis [17–19]. These antibodies have been further utilized in passive immunization experiments to evaluate the role of Fc receptors (FcRs) and complement in RBC:autoantibody immune complex clearance and pathology [20,21].
Recent findings: oxidative stress may be a risk factor for autoimmune hemolytic anemia
More recent studies with the NZB murine model have focused on the correlation between oxidative stress and AIHA. Analysis of RBCs from NZB mice have demonstrated elevated levels of intracellular reactive oxygen species (ROS) compared to nonautoimmune prone mice [22,23]. Intriguingly, as NZB RBCs age, levels of intracellular ROS production increase, and erythrocytes display higher levels of methemoglobin and lipid peroxidation – metrics associated oxidative stress. The degree of RBC oxidative stress was directly correlated with autoantibody production and anemia. Moreover, prevention of AIHA in NZB mice was achieved through overexpression of superoxide dismutase 1 (SOD1), an enzyme that breaks down free radicals such as ROS, thereby demonstrating a direct role of oxidative stress and AIHA onset [22,24,25,26▪]. These studies lend additional insight and importance to the role of oxidative stress and RBC survival. Moreover, these findings complement observations in human blood storage biology that show some individuals have RBCs that exhibit oxidative stress markers upon storage, which, in turn, may negatively impact posttransfusion RBC survival . Thus, given the emergence of mass spectrometry analysis in transfusion medicine research, metabolomics and blood storage biology may provide key knowledge into AIHA pathogenesis (and autoimmunity in general) and provide a foundation to evaluate ways to prevent harmful oxidative damage and reverse the course of autoimmunity.
PLAYFAIR AND MARSHALL–CLARKE MODEL: EXPERIMENTALLY INDUCED AUTOIMMUNE HEMOLYTIC ANEMIA
Summary of previous findings
Autoimmune hemolytic anemia can be induced in mice by weekly intraperitoneal injection of rat RBCs, commonly referred to as the Playfair and Marshall–Clarke model . Erythrocyte autoantibodies are detectable within 5–6 weeks and correlate with a shortened RBC lifespan and a significant drop in hematocrit and hemoglobin . Similar to observations with the NZB murine model, predisposition to AIHA involves genetics, gender, and dysregulation of cytokines [30–33]. Distinctly, findings in this model have elucidated that T cell immune responses to RBC-derived antigens are cross-reactive between species and that linked recognition of foreign rat RBC-derived epitopes provide help to murine RBC autoreactive B cells and can induce AIHA [34–36]. Additionally, this model of AIHA has been instrumental in demonstrating a key role of regulatory T cells in modulating RBC autoimmunity [37,38].
Recent findings: pathogenic antierythrocyte autoantibodies target reticulocytes
Most recently, the use of the Playfair and Marshall–Clarke model has been utilized to study how pathogenic autoantibodies affect RBCs. Saxena et al. has developed a technique called double in-vivo biotinylation (DIB) to delineate erythrocyte age, which has been instrumental in elucidating age-related changes and clearance. Incorporation of DIB in multiple models of anemia has demonstrated that clearance patterns of RBC precursors, reticulocytes, and mature RBCs are distinct, depending on how anemia is induced (e.g., heavy metal, autoantibodies) [39,40▪]. With regard to the Playfair and Marshall–Clarke model, reticulocytes have more autoantibodies bound to their surface, produce more ROS, and are preferentially cleared from circulation [41▪]. Moreover, injection of pathogenic autoantibodies (from rat RBC-induced AIHA mice) into DIB-treated naïve mice leads to an accumulation of autoantibodies and phosphatidylserine exposure on reticulocytes, thereby demonstrating that autoantibody binding induces changes in the RBC membrane, which ultimately affect clearance [42▪▪]. Thus, the DIB technique has allowed for additional insight into AIHA sequelae and demonstrate that reticulocytes are most susceptible to the effects of pathogenic autoantibodies. Furthermore, these studies demonstrate interconnectivity between the effects of pathogenic autoantibody binding of RBCs, FcR-mediated erythrophagocytosis, and AIHA pathogenesis; additional extension of studies with the DIB technique may help parse out how different autoantibody subtypes modulate RBC membranes, clearance, and hemolysis.
TRANSGENIC MODELS OF AUTOIMMUNE HEMOLYTIC ANEMIA: HEAVY AND LIGHT (HL) AND HEN EGG LYSOZYME, OVALBUMIN, DUFFY (HOD) MICE
The first murine transgenic model of autoimmune hemolytic anemia, HL mice
Okamoto and colleagues generated HL transgenic mice, in which all B cells express the same B cell receptor comprises the heavy and light chain (HL) from monoclonal antibody 4C8, derived from NZB mice . 4C8 has been described as a pathogenic immunoglobulin M (IgM) antibody that recognizes Band 4.1, and upon passive immunization, causes anemia and agglutination of RBCs in the spleen and liver . Transgenic HL mice experience a range of AIHA symptoms from tolerance to severe anemia, depending on the state of inflammation and housing conditions [44,45]. Analysis of HL mice has revealed that B cell tolerance is abnormal; conventional RBC autoreactive B cells undergo deletion or anergy, whereas anti-RBC innate B-1 B cells in the peritoneal cavity and lamina propia are enriched . Additionally, there is a correlation between deletion-resistant B-1 B cells and production of antierythrocyte antibodies. Polyclonal activation of peritoneal B cells with lipopolysaccharide prompts B cell proliferation, an increase in autoantibody production, and exacerbates anemia . In contrast, intraperitoneal injection of deionized water or autoantigen-expressing RBCs initiate B-1 B cell apoptosis and lead to amelioration of AIHA symptoms [47–49]. Thus, data from this model supports a pool of autoreactive anti-RBC B cells that, by existing in extramedullary spaces, has escaped tolerance mechanisms and maintain capacity to secrete autoantibodies. The HL model provided the foundation for the prevailing paradigm of B cell tolerance to RBC autoantigens for almost two decades.
HOD model of red blood cell tolerance and autoimmunity
The AIHA models described above have generated significant knowledge and understanding of AIHA pathogenesis; however, there are several limitations to using these models as a platform to study the disease initiation and broader concepts of tolerance and autoimmunity to erythrocyte antigens. The biggest challenge is the absence of tools and reagents specific for these models such that we can extract more mechanistic understanding. To overcome these limitations, a new murine model for RBC tolerance and autoimmunity was developed: the HOD mouse (Fig. 1a). HOD mice express an RBC-restricted triple fusion protein consisting of hen egg lysozyme (HEL), ovalbumin (OVA), and human blood group molecule, Duffy (HOD) . The combination of these proteins takes advantage of the currently available tools and reagents that enable the dissection of the immune response, including
- well described proteins with B and T cell antigens (HEL and OVA, respectively)
- OVA-specific tetramers which allow for identification of OVA-reactive T cells
- tetramerized HEL to identify HEL-specific B cells
- Transgenic animals: OTII (CD4 T cells that recognize OVA presented by I-Ab), 3A9 (CD4 T cells that recognize OVA presented by I-Ak), OTI (CD8 T cells that recognize OVA presented by Kb), IgHEL (also called MD4, B cells that recognize HEL), SwHEL (B cells that recognize HEL)
- monoclonal antibodies that recognize HEL, OVA, and Duffy
Analysis of naïve HOD mice has demonstrated that tolerance to RBC-specific antigens is robust; immunization with either HEL or OVA proteins emulsified in CFA is not sufficient to break tolerance and lead to autoantibody production . This observation is consistent with those of the Playfair and Marshall–Clarke model as induction of anemia is dependent on cross-reactivity of foreign and self-epitopes and, possibly, linked recognition. Moreover, autoreactive lymphocytes are detectable in HOD mice. Autoreactive B cells persist despite central and peripheral tolerance mechanisms and, upon adoptive transfer of HOD-reactive CD4 T cells, are stimulated to secrete autoreactive antibodies . These findings also align with observations made with NZB, Playfield and Marshall–Clarke, and HL models of AIHA as all mice make detectable autoantibodies, which demonstrate that erythrocyte-specific autoreactive B cells are present in the periphery and retain the capacity to secrete autoantibodies. Thus, T cell tolerance is a stopgap to autoimmunity. Indeed, while autoreactive CD4 T cells are detectable in the periphery of HOD mice, they are nonfunctional. Intriguingly, and in contrast to the Playfield and Marshall–Clarke model, despite the presence of autoreactive T cells expressing a CD4+CD25+FoxP3+ regulatory phenotype, depletion of Tregs in HOD mice did not lead to autoimmunity [52▪]. Thus, the HOD model shares common themes with currently described models of AIHA and provides additional evidence to support the hypotheses that linked recognition and dysregulation of lymphocyte activation are risk factors for AIHA.
Based on the observations made with all AIHA models, it has become clear that tolerance to RBC antigens, especially those restricted to RBCs, is not complete; autoreactive lymphocytes are detectable in the periphery, receptive to activating signals, and can perpetuate an autoimmune response. These data are consistent with observations made in humans as tolerance to RBCs breaks down frequently; 0.1% of asymptomatic blood donors have detectable autoantibodies on their erythrocytes and this frequency increases to 7% in hospitalized patients [53–55]. Thus, given the functional importance of RBCs (e.g., tissue oxygenation and hemostasis), how are lymphocytes tolerized to erythrocyte antigens?
Are B cells educated against red blood cell-restricted antigens?
Innate B-1 B cells represent a distinct population of B cells; in general, they are polyreactive, express/secrete (mostly) IgM, utilize restricted variable, diversity, joining (VDJ) genes for their B cell receptor (BCR), and are positively selected for during development by strong BCR:self-antigen signals . NZB and HL models of AIHA implicate B-1 B cells as the source of RBC autoantibodies, whereas conventional autoreactive B-2 B cells undergo deletion or anergy . However, these results have recently been challenged by use of the HOD model in which HOD mice were crossed to two different BCR transgenic (Tg) mice (IgHEL and SwHEL) [57▪▪]. Both BCR Tg mouse lines express the same paratope specific for HEL but the IgHEL mouse was generated via a random transgenic approach in which the IgHEL is expressed as an IgM and with allelic suppression of background immunoglobulin G (IgG) recombination, whereas the SwHEL mouse was made with VDJ knock-in technology allowing normal class switching [58,59]. As such, the IgM-restricted IgHEL mouse cannot undergo BCR rearrangement, receptor editing, or class-switching. Analysis of bone marrow and splenocytes of autoreactive HOD+IgHEL+ mice have shown that B-2 B cells are deleted in the lymphoid organs, B-1 B cells are enriched in the peritoneum, and mice had detectable IgM autoantibodies that correlated with mild anemia. These observations are consistent with those made with HL transgenic mice, which are (like IgHEL) cannot class switch. In contrast, while HOD+SwHEL+ mice make HOD-specific autoantibodies, both B-1 and B-2 B cell subsets undergo significant deletion in this model. These findings demonstrate that B cells are educated against RBC self-antigens early during development, as evidenced by deletion of autoreactive B cells. Moreover, they suggest that B cells require receptor rearrangement and editing (available in SwHEL but not IgHEL or HL BCR Tg mice) for tolerance mechanisms to be effective. It is worth noting, however, B cell tolerance is incomplete as autoantibodies are present in both HOD+IgHEL+ and HOD+SwHEL+ mice. These studies highlight the importance of how BCR Tg mice are constructed, as very different results are obtained in each cross. Importantly, these data challenge the existing paradigm that B-1 B cells are solely responsible for erythrocyte autoantibodies.
How are T cells tolerized to red blood cell-specific autoantigens?
Evidence from analysis of naïve HOD mice has demonstrated that T cells are the stopgap to autoimmunity in the HOD model. Wong et al. recently described a model of AIHA using the F1 of HOD and OTII mice (OTII mice are CD4 T cell receptor transgenic mice that recognize OVA contained within the HOD triple fusion RBC antigen) (AABB oral abstract; 2017). Analysis of these mice has shown that autoreactive thymic T cells are neither deleted nor diverted into Tregs, indicating that central tolerance to an RBC-specific antigen (HOD) is not present in these animals and suggesting that RBC autoantigens are not presented in the thymus. Younger HOD+OTII+ mice do not have detectable autoantibodies; however, upon aging, a subset of mice displayed symptoms of AIHA with detectable HOD-specific autoantibodies, decreased hematocrit, splenomegaly, and increased frequency of RBC precursors. Additionally, these studies mirror characteristics observed in human patients with AIHA and autoimmunity in general – female predominance, age-related onset, and two groups of autoantibody producers: relapse-remitting and low-level sustained. Thus, these findings show that T cells can be tolerized to erythrocyte antigens; and, although peripheral tolerance mechanisms may be more critical than thymic central tolerance, tolerance can break down and lead to AIHA.
Advantages and limitations to the HOD model
The HOD model of erythrocyte autoreactivity has proven to be a powerful platform to dissect how the immune system responds to antigens on RBCs and will likely continue to provide fruitful information. Similar to HL Tg mice, the autoantibody target in HOD mice is RBC-restricted, making both models relevant to AIHA studies as the most frequently targeted antigens in human patients are those with limited expression patterns (e.g., the Rh complex, Band 3). By crossing HOD mice with BCR and TCR Tg mice, it has been possible to recapitulate the HL Tg model whereby autoreactive lymphocytes are present and AIHA symptoms develop. However, the advantage of the HOD model over the HL Tg model is that the HOD transgene is not a critical component to RBC structure or function; thus, it is possible to allow for characterization of Tg B and T cells in the absence of their autoantigen (i.e., HOD-OTII+ or HOD-IgHEL+ or HOD-SwHEL+ mice). In contrast, HL Tg mice express a BCR specific against Band 4.1 and, while Band 4.1 knockout mice have been generated, they develop AIHA and their RBCs are unstable. Thus, analysis of the BCR Tg in the absence of their autoantigen could not be accomplished. As such, the observation that IgM-restricted peritoneal B-1 B cells were responsible for antierythrocyte autoantibodies is a direct result of how the BCR Tg mouse was constructed. Moreover, despite autoantibody generation in the HOD model, HOD mice experience only mild anemia (like the vast majority of autoantibodies to RBCs in humans); thus, studying how tolerance breaks down and the subsequent mechanism of RBC clearance and immunity is easier to study as there is no confounding pathology associated with chronic hemolysis. Finally, by crossing the HOD mouse with BCR and TCR Tg animals, it is now possible to dissect how autoreactive lymphocytes are tolerized to RBC antigens thereby allowing for identification of when and where RBC autoantigens are encountered.
There are limitations to the HOD model, however. Akin to many other RBC antigens, some antibodies generated against the HOD antigen do not induce hemolysis but promote antigen-modulation. While this provides an opportunity to study the mechanisms of antigen-modulation and may allow for insight into the key characteristics of an antibody that promotes antigen-modulation versus hemolysis; it also confounds the observed results. Of greater concern with use of the HOD model is that, when combined with the BCR and TCR Tg mice, the autoreactive lymphocytes have a strong affinity to their cognate antigen; thus, these studies could represent the extreme spectrum of immune responses. This can be remedied in future experiments by altering the sequences of HEL and/or OVA in the HOD molecule, such that affinity is less. Nonetheless, the HOD model of erythrocyte autoreactivity provides an opportunity to elucidate the mechanisms of tolerance and autoimmunity to RBC autoantigen that may inform future therapies for AIHA patients.
The past 2 decades have seen rapid advancement in genomics, proteomics, and metabolomics. The application of these approaches to study RBC biology will likely continue to provide significant information about how RBCs respond to environmental cues (e.g., exposure to ROS), provide insight into potential therapies to reverse and/or mitigate the harmful effects of oxidative stress on RBCs, and contribute considerable knowledge to understanding how RBCs are affected by autoantibody binding. Moreover, there is potential to extend these findings into RBC storage biology and alloimmunization. Given our recent technological advances, It is now possible to explore the relationship between AIHA onset and microbiome composition, lymphocyte tolerance mechanisms, and autoantibody sequence and functional characteristics that will provide answers to many outstanding questions:
- What are the mechanisms of T cell tolerance employed against RBC antigens?
- How does RBC-specific T cell tolerance break down? Can it be prevented or reversed?
- Does RBC antigen density or expression pattern play a role in tolerance breakdown?
- Can the microbiome predispose an individual to develop AIHA?
- How does RBC hemolysis affect the microbiome?
- Why do some autoantibodies induce hemolysis whereas others do not?
Autoimmune hemolytic anemia is a severe, and sometimes fatal, disease. Treatment options are limited and sometimes ineffective. And, while much knowledge is known about the destructive effects of pathogenic autoantibodies, there is still much to learn about why and how autoantibodies are generated. Additional studies with new transgenic murine models in RBC transfusion will provide additional insight into how tolerance to RBCs is established, maintained, and broken down; these studies will lead to new understanding into AIHA initiation and provide a foundation to generate new, more effective, treatment options.
The authors would like to thank Drs Jeanne E. Hendrickson, Christopher Tormey, and James C. Zimring for critical review of this manuscript.
Financial support and sponsorship
This work was supported, in part, by the National Blood Foundation and a grant from the National Institutes of Health (NIH NHLBI 1R01HL133325).
Conflicts of interest
There are no conflicts of interest.
REFERENCES AND RECOMMENDED READING
Papers of particular interest, published within the annual period of review, have been highlighted as:
- ▪ of special interest
- ▪▪ of outstanding interest
1. Shulman IA, Branch DR, Nelson JM, et al. Autoimmune hemolytic anemia
with both cold and warm autoantibodies. JAMA 1985; 253:1746–1748.
2. Chaudhary RK, Das SS. Autoimmune hemolytic anemia
: from lab to bedside. Asian J Transfus Sci 2014; 8:5–12.
3. Packman CH. The clinical pictures of autoimmune hemolytic anemia
. Transfus Med Hemother 2015; 42:317–324.
4. Fung MK, Eder AF, Spitalnik SL, Westhoff CM. Technical Manual of the Americal Association of Blood Banks. AABB, 19th edition.Bathesda, Maryland: 2017.
5. Reynaud Q, Durieu I, Dutertre M, et al. Efficacy and safety of rituximab in auto-immune hemolytic anemia: a meta-analysis of 21 studies. Autoimmun Rev 2015; 14:304–313.
6. Go RS, Winters JL, Kay NE. How I treat autoimmune hemolytic anemia
. Blood 2017; 129:2971–2979.
7. Lechner K, Jäger U. How I treat autoimmune hemolytic anemias in adults. Blood 2010; 116:1831–1838.
8. Helyer B, Howie J. Spontaneous auto-immune disease in NZB/BL mice. Br J Haematol 1963; 9:119–131.
9. Howie JB, Helyer BJ. The immunology and pathology of NZB mice. Adv Immunol 1968; 9:215–266.
10. Ghaffar A, Playfair JH. The genetic basis of autoimmunity
in NZB mice studied by progeny-testing. Clin Exp Immunol 1971; 8:479–490.
11. Warner NL. Genetic control of spontaneous and induced antierythrocyte autoantibody production in mice. Clin Immunol Immunopathol 1973; 3:353–363.
12. Knight JG, Adams DD. Genes determining autoimmune disease in New Zealand mice. J Clin Lab Immunol 1981; 5:165–170.
13. Ozaki S, Honda H, Maruyama N, et al. Genetic regulation of erythrocyte autoantibody production in New Zealand black mice. Immunogenetics 1983; 3:241–254.
14. Chiang BL, Bearer E, Ansari A, et al. The BM12 mutation and autoantibodies to dsDNA in NZB.H-2bm12 mice. J Immunol 1990; 145:94–101.
15. Naiki M, Yoshida SH, Watanabe Y, et al. The contribution of I-Abm12 to phenotypic and functional alterations among T-cell subsets in NZB mice. J Autoimmun 1993; 6:131–143.
16. Russell PJ, Cunningham J, Dunkley M, et al. The role of suppressor T cells in the expression of autoimmune haemolytic anaemia in NZB mice. Clin Exp Immunol 1981; 45:496–503.
17. de Sá Oliveira GG, Izui S, Ravirajan CT, et al. Diverse antigen specificity of erythrocyte-reactive monoclonal autoantibodies from NZB mice. Clin Exp Immunol 1996; 105:313–320.
18. Izui S, Reininger L, Shibata T, Berney T. Pathogenesis of autoimmune hemolytic anemia
in New Zealand black mice. Crit Rev Oncol Hematol 1994; 1:53–70.
19. Takakuwa Y. Protein 4.1, a multifunctional protein of the erythrocyte membrane skeleton: structure and functions in erythrocytes and nonerythroid cells. Int J Hematol 2000; 3:298–309.
20. Shibata T, Berney T, Reininger L, et al. Monoclonal antierythrocyte autoantibodies derived from NZB mice cause autoimmune hemolytic anemia
by two distinct pathogenic mechanisms. Int Immunol 1990; 2:1133–1141.
21. Baudino L, Fossati-Jimack L, Chevalley C, et al. IgM and IgA antierythrocyte autoantibodies induce anemia in a mouse model through multivalency-dependent hemagglutination but not through complement activation. Blood 2007; 109:5355–5362.
22. Iuchi Y, Kibe N, Tsunoda S, et al. Implication of oxidative stress as a cause of autoimmune hemolytic anemia
in NZB mice. Free Radic Biol Med 2010; 48:935–944.
23. Fujii J, Kurahashi T, Konno T, et al. Oxidative stress as a potential causal factor for autoimmune hemolytic anemia
and systemic lupus erythematosus. World J Nephrol 2015; 4:213–222.
24. Iuchi Y, Okada F, Onuma K, et al. Elevated oxidative stress in erythrocytes due to a SOD1 deficiency causes anaemia and triggers autoantibody production. Biochem J 2007; 402 (Pt 2):219–227.
25. Konno T, Otsuki N, Kurahashi T, et al. Reactive oxygen species exacerbate autoimmune hemolytic anemia
in New Zealand Black mice. Free Radic Biol Med 2013; 65:1378–1384.
26▪. Otsuki N, Konno T, Kurahashi T, et al. The SOD1 transgene expressed in erythroid cells alleviates fatal phenotype in congenic NZB/NZW-F1 mice. Free Radical Research 2016; 50:793–800.
Showed that SOD1 deficiency in NZBxNZW F1 mice lead to decreased murine lifespan and increased levels of ROS in erythrocytes and demonstrated that overexpression of human SOD1 rescued the phenotype.
27. Fu X, Felcyn JR, Odem-Davis K, Zimring JC. Bioactive lipids accumulate in stored red blood cells
despite leukoreduction: a targeted metabolomics study. Transfusion 2016; 56:2560–2570.
28. Playfair JH, Marshall-Clarke S. Induction of red cell autoantibodies in normal mice. Nat New Biol 1973; 128:213–214.
29. Cox KO, Keast D. Autoimmune haemolytic anaemia induced in mice immunized with rat erythrocytes. Clin Exp Immunol 1974; 17:319–327.
30. Cooke A, Playfair JH. Hyper-responsiveness in NZB mice to the experimental induction of antired cell autoantibody. Clin Exp Immunol 1977; 27:538–544.
31. Cooke A, Hutchings P. Sex differences in the regulation of experimentally induced autoantibodies in (NZB x NZW)F1 mice. Immunology 1980; 41:819–823.
32. Xu L, Zhang T, Liu Z, et al. Critical role of Th17 cells in development of autoimmune hemolytic anemia
. Exp Hematol 2012; 40:994.e4–1004.e4.
33. Dahal LN, Hall LS, Barker RN, Ward FJ, et al. Indoleamine 2,3 dioxygenase contributes to transferable tolerance
in rat red blood cell inducible model of experimental autoimmune haemolytic anaemia. Clin Exp Immunol 2013; 173:58–66.
34. Playfair JH, Marshall-Clarke S. Cross-reactions between erythrocytes at the T-cell level. Immunology 1973; 24:579–588.
35. Barker RN, Casswell KM, Elson CJ. Identification of murine erythrocyte autoantigens and cross-reactive rat antigens. Immunology 1993; 78:568–573.
36. Barker RN, Shen CR, Elson CJ. T-cell specificity in murine autoimmune haemolytic anaemia induced by rat red blood cells
. Clin Exp Immunol 2002; 129:208–213.
37. Cooke A, Hutchings P, Playfair JH. Suppressor T cells in experimental autoimmune haemolytic anaemia. Nature 1978; 5658:154–155.
38. Mqadmi A, Zheng X, Yazdanbakhsh K. CD4(+)CD25(+) regulatory T cells control induction of autoimmune hemolytic anemia
. Blood 2005; 105:3746–3748.
39. Saxena RK, Khandelwal S. Aging and destruction of blood erythrocytes in mice. Current Science 2009; 97:500–507.
40▪. IntechOpen, Chatterjee S, Saxena RK. Koopman-van Gemert AWMM. A double in vivo biotinylation technique to assess erythrocyte turnover in blood circulation. Transfusion Medical and Scientific Developments 2017.
Description and demonstration of a new biotinylation technique utilized to assess RBC age and turnover. Also described how anemia affects clearance of RBCs and their precursors.
41▪. Chatterjee S, Bhardwaj N, Saxena RK. Identification of stages of erythroid differentiation in bone marrow and erythrocyte subpopulations in blood circulation that are preferentially lost in autoimmune hemolytic anemia
in mouse. PLoS One 2016; 11:e0166878.
Utilization of the double in-vivo biotinylation to demonstrate that reticulocytes have increased autoantibodies on their surface, produce more ROS, and are preferentially cleared from circulation in the Playfair and Marshall-Clarke model of AIHA.
42▪▪. Chatterjee S, Saxena RK. Binding of autoantibodies and apoptotic response in erythroid cells in the mouse model of autoimmune hemolytic anemia
. Hematol Tranfus Int J 2017; 5:155.
Showed that anti-RBC pathogenic autoantibodies preferentially bind to reticulocytes and induce phosphatidylserine expression.
43. Okamoto M, Murakami M, Shimizu A, et al. A transgenic model of autoimmune hemolytic anemia
. J Exp Med 1992; 175:71–79.
44. Murakami M, Tsubata T, Shinkura R, et al. Oral administration of lipopolysaccharides activates B-1 cells in the peritoneal cavity and lamina propria of the gut and induces autoimmune symptoms in an autoantibody transgenic mouse. J Exp Med 1994; 180:111–121.
45. Murakami M, Nakajima K, Yamazaki K, et al. Effects of breeding environments on generation and activation of autoreactive B-1 cells in antired blood cell autoantibody transgenic mice. J Exp Med 1997; 185:791–794.
46. Murakami M, Honjo T. Antired blood cell autoantibody transgenic mice: murine model of autoimmune hemolytic anemia
. Semin Immunol 1996; 8:3–9.
47. Murakami M, Yoshioka H, Shirai T, et al. Prevention of autoimmune symptoms in autoimmune-prone mice by elimination of B-1 cells. Int Immunol 1995; 7:877–882.
48. Murakami M, Tsubata T, Okamoto M, et al. Antigen-induced apoptotic death of Ly-1 B cells responsible for autoimmune disease in transgenic mice. Nature 1992; 357:77–80.
49. Sakiyama T, Ikuta K, Nisitani S, et al. Requirement of IL-5 for induction of autoimmune hemolytic anemia
in antired blood cell autoantibody transgenic mice. Int Immunol 1999; 11:995–1000.
50. Desmarets M, Cadwell CM, Peterson KR, et al. Minor histocompatibility antigens on transfused leukoreduced units of red blood cells
induce bone marrow transplant rejection in a mouse model. Blood 2009; 114:2315–2322.
51. Hudson KE, Hendrickson JE, Cadwell CM, et al. Partial tolerance
of autoreactive B and T cells to erythrocyte-specific self-antigens in mice. Haematologica 2012; 97:1836–1844.
52▪. Richards AL, Kapp LM, Wang X, et al. Regulatory T cells are dispensable for tolerance
to RBC antigens. Front Immunol 2016; 7:348.
Demonstrated that CD25+FoxP3+ regulatory T cells (Tregs) are not required for maintenance of tolerance to the HOD RBC autoantigen and suggests that Tregs may not be required for prevention of erythrocyte autoimmunity.
53. Gorst DW, Rawlinson VI, Merry AH, Stratton F. Positive direct antiglobulin test in normal individuals. Vox Sang 1980; 38:99–105.
54. Stratton F, Rawlinson VI, Merry AH, Thomson EE. Positive direct antiglobulin test in normal individuals. II. Clin Lab Haematol 1983; 5:17–21.
55. Freedman J. False-positive antiglobulin tests in healthy subjects and in hospital patients. J Clin Pathol 1979; 32:1014–1018.
56. Baumgarth N. A Hard(y) look at B-1 cell development and function. J Immunol 2017; 199:3387–3394.
57▪▪. Richards AL, Howie HL, Kapp LM, et al. Innate B-1 B cells are not enriched in red blood cell autoimmune mice: importance of B cell receptor transgenic selection. Front Immunol 2017; 8:
Showed that RBC autoreactive B cells persist despite central tolerance mechanisms. Also demonstrated fundamental B cell development differences between B cell receptor knock-in and replacement transgenic animals.
58. Phan TG, Amesbury M, Gardam S, et al. B cell receptor–independent stimuli trigger immunoglobulin (Ig) class switch recombination and production of IgG autoantibodies by anergic self-reactive B cells. J Exp Med 2003; 197:845–860.
59. Hartley SB, Crosbie J, Brink R, et al. Elimination from peripheral lymphoid tissues of self-reactive B lymphocytes recognizing membrane-bound antigens. Nature 1991; 353:765–769.
Keywords:Copyright © 2018 Wolters Kluwer Health, Inc. All rights reserved.
autoimmune hemolytic anemia; autoimmunity; murine models of autoimmune hemolytic anemia; red blood cell autoantibodies; red blood cells; tolerance