Open access
1. Introduction
The microbe
However, it is intriguing to observe that the incidence and morbidity of the disease varies greatly in different regions of the globe, being highest in Africa and Asia, as well as the response to BCG vaccination [1,4]. That, in spite of the fact that there are no structurally variable strains of MTB, therefore all have a similar virulence capacity. One important factor is the introduction of the human immunodeficiency virus (HIV) into areas and populations already having a high TB incidence [5], the resulting double infections having a disastrous effect. This is especially prominent in sub-Saharan Africa. But that factor alone can not explain the global epidemiological variability in the disease. Also, why only one in ten carriers of the microbe become clinically sick?
In order to address these questions, in the present chapter we will try to delve into the intricacies of the human immune response to MTB infection and to explore possible differences in the genetic regulation of the host immune responses in various human populations.
2. The encounter of Mtb with the innate immune system
Most human infections with MTB occur through inhaled carrier droplets into the lower airways. There the microbe encounters the alveolar macrophage (AMac) and submucosal dendritic cell (DC). The outcome of the ensuing battle will determine whether the infection will remain locally limited within the engulfing cells of the innate immune system, or will continue to spread, causing the individual to become a clinically active TB patient [1,6,7,8]. During the first contact, the AMac recognizes the microbe through pattern recognition receptors (PRRs), which sense microbial biochemical components, such as outer coat mannosylated lipoarabinomannan (ManLam), trehalose dimycolate and N-glycolymuramyl dipeptide. These molecules act as pathogen-associated molecular patterns (PAMPs), which trigger an intracellular signaling cascade in the AMac, which leads to a phagocytic activity, which, if successful, will result into the complete engulfing of the microbe into cytosolic vesicles- the phagolysozomes and secretion of pro-inflammatory cytokines, such as tumor-necrosis factor alpha (TNFα). ManLam also binds directly to mannose receptors on macrophages and DCs.
The best studied PRRs are Toll-like receptors (TLRs) [6,9,10], of which 10 have been identified in humans. TLR- 2 and TLR-4 recognize bacterial products [9,11], TLR-2 having a major role in recognizing MTB in the lung. All contain an intracellular TIR domain, the activation of which initiates a signaling cascade via adapter proteins such as MyD88, interferon-inducing TRIF and TRIF-related adapter molecule TRAM, which results in the recruitment of interleukin-1(IL-1) receptor-associated kinase (IRAK) 4, which phosphorylates IRAK-1. The latter binds to TNFα receptor-associated factor (TRAF) 6, leading to kinase-dependent IkBα phosphorylation, the degradation of which leads to the activation of nuclear NF-kB, which is the main nuclear activator of proinflammatory cytokines. Another intracellular PRR is nucleotide-binding oligomerization domain 2 (NOD2), which binds bacterial cell-wall muramyl-dipeptide, eliciting secretion of TNFα, IL-1β, IL-6 and bacteridal LL-37 [12,13]
Neutrophils also play a defensive role, not only as first-line non-specific phagocytes, but also by secreting anti-bacterial proteins, mainly the cathelicidin LL-37 [1,14]. Neutrophils loaded by phagocytized bacteria become apoptotic, thereby eliciting macrophage activation [15].
NK cells, which are large granular circulating lymphocytes, are attracted to the sites of bacterial infections, where they specialize in recognizing and destroying infected host cells. During this process they secrete interferon gamma (IFNγ), which activates macrophages, inducing them to secrete the cytokines IL-12, IL-15 and IL-18, which activate CD8+T-cells, thus forming the link to the adaptive immune system [7,16]
The complement is the humoral arm of the innate immune system. It has been shown that M. bovis BCG may activate the three pathways of complement: the classical pathway by binding to the C1q protein, the lectin pathway by binding to the bacterial cell surface mannose-binding lectin (MBL) or L-ficolin and the alternate pathway through the deposition of C3b on the bacterial surface. Mtb can activate the classical and alternate pathways by binding C3. This enables complement to perform its major functions-microbial opsonization, microbial cell lysis through the formation of the attack complex and leukocyte recruitment by eliciting chemokine secretion [7,17].
Another recently discovered anti-microbial mechanism of phagocytic cells is the use of vital transition metals, such as iron, zinc and copper, to poison intracellular microorganisms. However, mycobacteria have developed a resistance mechanism to such intoxication [18,19]. This contrasts with the function of the phagosomal metal transporter natural resistance-associated membrane protein (NRAMP) 1 to deprive the microorganisms from essential nutrients, such as iron and manganese [20]. Such duality existing in the same cell is of interest.
Virulent Mtbs have acquired the capability to dampen the activity of NF-Kb by some of their antigens [6,7], such as ESAT-6 and ManLam. The latter also inhibits the secretion of IL-12, an essential cytokine in the anti-MTB inflammatory response. ESAT-6 downregulates MyD88- IRAK 4 interaction, thereby also interfering with TLR signaling to NFkB. A third antigen- CFP-10 markedly reduces nitric oxide (NO) and reactive-oxygen species (ROS) production by the macrophages, thereby inhibiting their non-specific killing ability. The microbe may also regulate macrophage apoptosis to its advantage and to inhibit IFNγ- mediated macrophage activation [7]. ESX is a recently discovered protein transport system through the outer membrane of the microbe, which is essential for its survival. It has been demonstrated, in an experimental model, that ESX-5 may modulate macrophage reactivity by dampening the inflammasome activation [21]. These mechanisms enable the microbe to survive in the macrophage phagosome in a balance which is precarious to the host. In addition Mtb may escape the phagolysozome into the cytosol by damaging its membrane. Most recently it has been described that the microbe may secrete toxins, such as the newly discovered MtpA protein, through its outer membrane into the macrophage cytosol, which may cause the death of the later by cell necrosis [22].
Vitamin D seems also to play an important role in the microbe-host pull-of-arms [23]. It may modulate the inflammatory effect of some metalloproteinases (MMPs) in the lung [24] and Vitamin D supplementation has hastened bacterial eradication in pulmonary tuberculosis in a clinical trial [25].
Thus, the encounter between MTB and the various components of the innate immune system induce a complicated and sophisticated series of host responses and counter responses by the microbe. The later is one of the most ancient human infections, carried by our ancestors since they fanned-out from Africa across the globe, therefore enabling it to adapt to the human immune response (26-Cole S, Tuberculosis in time and space, Econference).
However, the next long-term phase of the encounter is played by the activation of the adaptive immune system, as described in the next section.
3. The role of adaptive immunity in the outcome of the Infection
In the previous section the importance of the host innate immune response in the encounter with MTB was described. However, it is generally accepted that the long-term outcome of the primary infection is determined by the effective mobilization of the adaptive immune response. Active TB patients, as well as latently infected carriers, do not suffer from a general innate or adaptive immune defect. On the contrary, ex-vivo studies of their immunocyte function demonstrate increased lymphocyte proliferation and the secretion of numerous cytokines [27]. Thus the disease, in people generally healthy, is a result of a very specific immune failure in face of MTB, or other mycobacteria.
It was thought that the CD4+T cell is the omnipotent determinant of the adaptive immune response in TB. However, lately it became clear that more T-cell subsets, including CD8+ and TH17 cells and even B cells participate in the process [1,7,28]. The induction phase seems to be delayed relatively to the response to more common pathogens. It is initiated by signaling and presentation of the microbial peptides by the macrophages and DCs to the CD4+ cells via MHC class II molecules, while mycobacterial membranal lipids are presented through MHC-I molecules of the CD-1 family [29]. The presentation of mycobacterial antigens occurs within the draining lung lymph-nodes to which the macrophages have migrated, followed by the activation of CD4+ and other T cells. These T cells use various receptors, such as TLRs, NOD-like receptors and C-type lectins, for this purpose. The peptides considered as potentially immunodominant are the already mentioned ESAT-6 and CFP10 and others, such as Rv2031c, Rv2654c and Rv1038c. The T cell response to these antigens is not homogenous, various T cell epitopes being engaged during the different phases of the infection [30]. Other Rv proteins are binding to T cells mainly during the latent phase [31]. T cell activation, by the recognition of these antigens in the initiating phase, results in the secretion of numerous cytokines, mostly proinflammatory, such as IL-1β, IL-6, IL-21 and IL-12p40. The later activates CD4+TH1 cells, but p40 is also a subunit of IL-23, which induces the TH17 cell lineage, which secretes IL-17, IL-21 and IL-22. These cytokines are considered to be essential for anti-microbial protection and IL-17 is thought to have a major role in granuloma formation [32], as well as TNFα, which is also secreted by CD4+ cells and promotes intra-phagosomal killing of the bacteria in macrophages. During an acute mycobacterial infection γδ T cells secrete much IL-17 [33], which also promotes the secretion of IL-12, thus a self-enhancing inflammatory loop is being formed. This is balanced by the secretion of TGFβ, the role of which is to dampen an overreactive inflammatory response, partly so by inducing T-reg cells. The later may inhibit TH1 responses, thus potentially facilitating mycobacterial replication within macrophages [34]. A high incidence of T reg Foxp3 cells has been found in extra-pulmonary TB [35].
The activated T cells undergo clonal expansion and migrate out of the lymph nodes into the site of the infection in the lung, as effector T cells. This process is driven by chemokines, secreted by various inflammatory cells. Upon arrival to the battle ground they secrete interferon gamma (IFNγ), which is a key cytokine in the ensuing confrontation, by further activating the microbicidal machinery of the macrophage and causing it to secrete IL-18, amongst other cytokines, which seems to be part of the protective TH1 type response. IFNγ also induces the production of toxic NO via inducible NO synthase (iNOS). Casanova et al [36,37,38] have described in detail the importance of the IFNγ-IL-12 cytokines loop, including their receptors, for TB immunity. Furthermore they have described rare Mendelian genetic defects in this system, resulting in susceptibility to serious mycobacterial and sometimes salmonellar infections.
CD8+ T cells also participate in the immune reaction, as they have been found in the mediastinal lymph nodes, mixed with CD4+ cells and later at the infection site in the lungs. Most evidence about them has been collected in mouse and primate models and their role in human infections has not been fully elucidated [7].It has been demonstrated in vitro that CD8+ cells recognize bacterial peptides and lipids through the MHC-I CD-1 molecules, which induce a cytotoxic response toward the bacteria and to the phagocytes in which they reside. They also secrete IFNγ and TNFα. Humans with latent TB develop a high level of mycobacteria-specific CD8+ T cells [39].
From all the above it is clear that the dominant protective response in TB is Th1 type. However in multiple-drug resistant (MDR) [40] and in young children [41] there is a skewing towards a Th2 type response, with greater secretion of IL-4. This may explain why children tend to develop pulmonary milliary and extrapulmonary disease. In addition it seems that the disease in children tends to have a Mendelian heritability of specific defects, while in adults there is no such background, rather some discrete polymorphisms may be found in different populations, such as in the natural resistance-associated macrophage protein 1 (NRAMP1) [42].
For a long time it was generally accepted that B-cells and specific antibodies have no protective role against TB. However monoclonal antibodies against some mycobacterial antigens have shown a clear protective effect in mice [43]. It has been postulated that the unique phenomenon of BCG protection against pediatric TB meningitis may be due in part to specific antibodies. Presently the exact role of B-cells in human TB remains to be determined.
Similarly to the innate immune system, mycobacteria have also developed evasion tactics from the adaptive immune system [44]. They may interfere with the antigen presentation process, promote the secretion of IL-10 by T cells, thereby polarizing them toward a TH2 type response, in which the essential IFNγ secretion is inhibited [7]. They may also attract more T-reg cells to the infection site, thereby further dampening the protective inflammatory response. It was demonstrated in a tuberculosis rabbit model, that mycobacteria may delay the macrophage and T-cells activation process, thereby enabling them to form a permanent infection and damaging pulmonary tissue [45]. More specifically, the bacteria possess a set of genes- rpf, which code for the regulatory Rpf proteins, which are believed to be responsible for activating bacteria from a dormant state in latency. In addition the bacteria have also a set of “anti-dormancy genes”-DosR, which induce bacterial growth, when appropriate [46].
4. The tuberculous granuloma
The formation of granuloma is the host’s containment effort in response to an infection which he can not eradicate. In most cases it results in a state of latency, with dormant, but viable, bacteria residing in it [7, 45, 47]. Therefore the granuloma benefits also the bacteria, who may emerge from dormancy, proliferate again and cause an active disease, if the host’s immune system is weakened due to any reason. HIV coinfection, with its damage to T cells, has become the most prominent example of this situation.
The granuloma contains a nucleus of necrotic lung tissue and intraphagosomal bacteria-containing macrophages, surrounded by fibroblasts, DCs, neutrophils, B cells and various subsets of T cells, all of those secreting cytokines, mainly IFNγ and TNFα, and chemokines which ensure a continuous mobilization of granulocytes to the granuloma. TNFα activates adhesion molecules on the immunocytes [48]. Thus the granuloma is a dynamic and continuous battlefield balancing the bacteria against the immune system. Occasionally, as described before, the bacteria may damage the phagosomal membrane and escape, inducing an apoptotic or necrotic death of the macrophage. This enables the bacteria to proliferate with enhancement of tissue damaging inflammation, which may result in cavity formation.
5. Shall we ever have an effective immunotherapy or anti-TB vaccine?
Application of highly effective vaccines across the globe is the only way to control and arrest the spread of infectious diseases. So far BCG is the only available anti-TB vaccine. It is one of the oldest vaccines and has remained unchanged for a long time. It does confer reasonable protection to infants at risk and prevents pediatric TB meningitis. However it is ineffective for protection of large adult populations and has failed to prevent the rise in new infections and active disease patients and especially in MDR and extreme drug resistant (XDR) cases [49]. Therefore many efforts have been invested in trying many forms of various extracts of other mycobacteria, such as M. vaccae, which may be considered as immunostimulants of TH1 responses or a kind of vaccines. Most have resulted in a transient enhancement of the anti-tuberculous inflammatory response, sometimes with severe side-effects, but without long-term clinical benefit [50]. How can this be explained?
The main reason is that decades of research have not, as yet, demonstrated a universal clearly immunodominant and protective T cell epitope to one of the bacterial antigens- mainly to cell-wall peptides, lipids or glycolipids. An exception may be the 85A and 85B antigens, which may be suitable candidates for a widely used anti-tuberculous vaccine under various constructs [51]. They show enhancement of TH1-type responses, but long-term clinical results are still unknown. Additional vaccines are under trials, such as MTB subunit and DNA preparations [52].
In addition there is the problem in the variability of the host immunogenetic response, both to BCG and to MTB [53]. Therefore various research projects are trying to identify, already mentioned, polymorphisms in immune-associated and other genes, which may increase or decrease the susceptibility to TB, such as the one which has been recently identified in a Moroccan population [54] and another one in a Chinese ethnic group [55]. This subject lies outside of the scope of this chapter, but it may lead to a better understanding of the processes determining the fate of a MTB infection and assist in designing better vaccines, although they may need to be population-targeted.
6. Summary
It has been attempted, in the present chapter, to describe in some detail the arms race between MTB and its ancient human host, who uses the full scope of his sophisticated innate and adaptive immune mechanisms to placate the enemy. The bacteria, which succeed to break the physical barriers in the respiratory tract and reach the lung, are immediately surrounded by residing DCs and AMa, which recognize the bacterial PAMPs with their PRRs, such as surface TLRs. This recognition triggers DC and macrophage activation, which results in the phagocytosis and internalization of the bacteria in the phagolysosome, where they are submitted to toxic lysis. Meanwhile the macrophages emigrate to the mediastinal lymph nodes, where the bacterial lipid and peptide molecules are presented to CD4+ and CD8+ T cells via MHC-I and MHC-II, causing T cell activation and clonal proliferation. The later return to the battlefield at the site of the lung infection and try to complete bacterial elimination, by intensifying local inflammation. To achieve that, the T cells and the macrophages secrete a series of cytokines, such as IFNγ, IL-12 and TNFα. Secreted chemokines attract more inflammatory cells, such as neutrophils.
Nevertheless, 90% of infected persons, who remain clinically asymptomatic, enter the stage of latency, in which they continue to harbor dormant, albeit viable, bacteria in their macrophages and 10% develop active clinical disease. This is due to numerous evasion tactics from the immune system, that MTB has developed during its long cohabitation with the human host. The bacterium may damage the phagosomal membrane and escape into the macrophage cytosol, inducing necrotic cell death. It may interfere with the signaling to T cells via MHC molecules, downregulate the secretion of IFNγ, promote the secretion of IL-10 and the activity of CD4+Foxp3 T reg cells, thus dampening the protective inflammatory response. A hallmark of the latency stage is granuloma formation, which is a complex structure, containing a core of dormant bacteria in necrotic tissue, surrounded by neutrophils, macrophages, DCs and T cells. This precarious balance may be easily disrupted, if, for whatever reason, immune surveillance is weakened, causing bacterial breakthrough and clinical relapse.
So far, BCG is the only antituberculous vaccine widely available, which does confer a measure of protection in children, but failed to arrest the spread of the infection in adult populations. Many centers around the world are trying to identify immunodominant bacterial epitopes, which could form the basis of a universal efficacious vaccine. So far, the 85A and 85B antigens, in various constructs, seem to be presently the most promising, at least in animal models and limited clinical trials. In addition, since the beginning of the 20th century, many mycobacterial formulations and lately also cytokines, have been tried as specific immune stimulants. In most cases they did induce generalized inflammation with significant side-effects, but with little clinical benefit. However, recent technological developments, such as recombinant preparations and DNA extracts, may obtain better results. To those have to be added numerous projects trying to unravel the immunogenetic susceptibility or resistance factors.
One may estimate that within a decade, or so, better anti-tuberculous vaccines and treatments will be developed, possibly targeted to specific populations.
References
- 1.
Lawn SD, Zumla AI, Tuberculosis. Lancet (Seminar) March 18, 2011, DOI:10.1016/S0140-6736(10)62173-3. - 2.
Dye C, Williams BG, The population dynamics and control of tuberculosis. Science 2010; 328:856-861. - 3.
WHO. Global tuberculosis control. Geneva: World Health Organization, 2010. http://www.whqlibdoc.who.int/publications/2010. - 4.
Brewer TF, Preventing tuberculosis with BCG vaccine: a metaanalysis of the literature. Clin Infect Dis 2000; 31(Suppl.3) S64-S67. - 5.
Getahun H, Raviglione M, Varma JK et al, CDC Grand Rounds: The TB/HIV syndemic. Morbidity & Mortality Weekly Reports 2012; 61(26):484-489. - 6.
Natarajan K, Kundu M, Sharma P, Basu J, Innate immune responses to M. tuberculosis infection. Tuberculosis 2011; 91:427-431. - 7.
Gupta A, Kaul K, Tsolaki AG et al, Mycobacterium tuberculosis: Immune evasion,latency and reactivation. Immunobiology 2012; 217:363-374. - 8.
Bafica A, Aliberti J, Mechanisms of host protection and pathogen evasion of immune responses during tuberculosis, in Alberti J (Ed), Control of Innate and Adaptive Immune Responses during Infectious Diseases, DOI 10,1007/978-1-4614-04842_2, Springer Science+Business Media,LLC 2012. - 9.
Ishii KJ, Koyama S, Nakagawa A et al, Host innate immune receptors and beyond: making sense of microbial infections. Cell Host Microbe 2008; 3:352-363. - 10.
Jenkins KA, Mansell A, TIR-containing adaptors in Toll-like receptor signaling. Cytokine 2010; 49:237-244. - 11.
Casanova JL, Abel L, Quintana-Murci L, Human TLR and IL-1Rs in host defence: natural insights from evolutionary, epidemiological and clinical genetics. Annu Rev Immunol 2011; 29:447-491. - 12.
Brooks MN, Rajaram MVS, Azad AK et al, NOD2 controls the nature of the inflammatory response and subsequent fate of Mycobacterium tuberculosis and M. bovis in human macrophages. Cell Microbiol 2011; 13(3):402-418. - 13.
Juarez E, Carranza C, Hernandez-Sanchez F et al, NOD2 enhances the innate response of alveolar macrophages to Mycobacterium tuberculosis in humans. Eur J Immunol 2012; 42:880-889. - 14.
Martineau AR, Newton SM, Wilkinson K et al, Neutrophil-mediated innate immune resistance to mycobacteria. J Clin Invest 2007; 117:1988-1994. - 15.
Persson YA, Blomgran-Julider R, Rahman S et al, Mycobacterium tuberculosis-induced apoptotic neutrophils trigger a pro-inflammatory response in macrophages through release of heat-shock protein 72, acting in synergy with the bacteria. Microbes Infect 2008; 10:233-240. - 16.
Vankayalapati R, Barnes PF, Innate and adaptive immune responses to human Mycobacterium tuberculosis infection. Tuberculosis 2009; 89 (Suppl1):577. - 17.
Carroll MV, Lack N, SimE et al, Multiple routes of complement activation by Mycobacterium bovis BCG. Mol Immunol 2009; 46:3367. - 18.
Botella H, Stadthagen G, Lugo-Villarino G et al, Metallobiology of host-pathogen interaction: an intoxicating new insight. Trends in Microbiol 2012; 3(3):106-112. - 19.
Rowland JL, Niederweis M, Resistance of Mycobacterium tuberculosis against phagosomal copper. Tuberculosis 2012; 92:202-210. - 20.
Fortier A et al, Single gene effects in mouse models of host-pathogen interactions. J Leukoc Biol 2005; 77:868-877. - 21.
Bottai D, Di Luca M, Majlessi L et al, Disruption of the ESX-5 system of Mycobacterium tuberculosis causes loss of PPE protein secretion , reduction of cell wall integrity and strong attenuation. Mol Microbiol 2012; 83:1195-1209. - 22.
Niederweis M, Death by Mycobacterium tuberculosis. EMBO conference on Tuberculosis 2012, Pasteur Institute, Paris, Sept. 2012. - 23.
Baeke F, Takiishi T, Korf H, Gysemans C, Mathieu C, VitaminD : modulator of the immune system. Curr Opin Pharmacol 2010; 10:482-496. - 24.
Prabhu-Anand S, Selvaraj P, Effect of 1,25 dihydroxyvitamin D3 on matrix metalloproteinases MMP-7,MMP-9 and the inhibitor TIMP-1 in pulmonary tuberculosis. Clin Immunol 2009; 133:126-131. - 25.
Martineau AR, Timms PM, Bothamley GH, High-dose vitamin D3 during intensive-phase antimicrobial treatment of pulmonary tuberculosis: a double-blind randomized controlled trial. Lancet 2011; 377:242-250. - 26.
Cole S, Tuberculosis in time and space. EMBO conference on Tuberculosis 2012, Pasteur Institute, Paris, Sept. 2012. - 27.
Handzel ZT, Barak V, Altman Y et al, Increased Th1 and Th2 type cytokine production in patients with active tuberculosis. IMAJ 2007; 9:479-483. - 28.
Philips JA, Ernst JD, Tuberculosis pathogenesis and immunity. Annu Rev Pathol 2012, 7:353-384. - 29.
Neyrolles O, Guilhot C, Recent advances in deciphering the contribution of Mycobacterium tuberculosis lipids to pathogenesis. Tuberculosis 2011, 91:187-195. - 30.
Arlehamn CSL, Sidney J, Henderson R et al, Dissecting mechanisms of immunodominance to the common tuberculosis antigens ESAT-6, CFP10,Rv2031c (hspX), Rv2654c TB7.7) and Rv1038c (EsxJ). J Immunol 2012; 188:5020-5031. - 31.
Schuck SD, Mueller H, Kunitz F et al, Identification of T-cell antigens specific for latent Mycobacterium tuberculosis infection. PLoS One 2009; 4:e5590. - 32.
Torrado E, Cooper AM, IL-17 and Th17 cells in tuberculosis. Cytokine Growth Factor Rev 2010; 21:455. - 33.
Peng M, Wang Z, Yao C et al, Interleukin 17-producing γδ T cells increased in patients with active pulmonary tuberculosis. Cell Mol Immunol 2008; 5(3):203-208. - 34.
Marin ND, Paris SC, Velez VM et al, Regulatory T cell frequency and modulation of IFNγ and IL-17 in active and latent tuberculosis. Tuberculosis 2010; 90:252. - 35.
Almeida de AS, Fiske CT, Sterling TR, Kalams S, Increased frequency of regulatory T cells and T lymphocyte activation in persons with previously treated extrapulmonary tuberculosis. Clin Vaccine Immunol 2012; 19:45-52. - 36.
Casanova JL, Abel L, Human genetics of infectious diseases: a unified theory. EMBO Journal 2007; 26:915-922. - 37.
Al-Muhsen S, Casanova JL, The genetic heterogeneity of mendelian susceptibility to mycobacterial diseases. J Aller Clin Immunol 2008; 122:1043-1051. - 38.
Rezaei N, Aghamohammadi A, Mansouri D et al, Tuberculosis: a new outlook at an old disease. Expert Rev Clin Immunol 2011; 7(2):129-131. - 39.
Ernst JD, The immunological life cycle of tuberculosis. Nat Rev Immunol 2012; 12(8):581-590. - 40.
Tan Q, Xie WP, Min R et al, Characterization of Th1 and Th2-type immune response in human multidrug resistant tuberculosis. Eur J Clin Microbiol Infect Dis 2012; 31(6):1233-1242. - 41.
Basu-Roy R, Whittaker E, Kampmann B, Current understanding of the immune response to tuberculosis in children; in: Heath PT (Ed), Paediatric and Neonatal Infections, Curr Opin Infect Dis 2012; 25(3):250-257. - 42.
Alcais A, Fieschi C, Abel L, Casanova JL, Tuberculosis in children and in adults: two distinct genetic diseases. J Exp Med 2005; 202(12):1617-1621. - 43.
Chambers MA, Gavier-Widen D, Hewinson RG, Antibody bound to the surface antigen MPB83 of Mycobacterium bovis enhances survival against high dose and low dose challenge. FEMS Immunol Med Microbiol 2004, 93. - 44.
Cooper AM, Torrado E, Protection versus pathology in tuberculosis: recent insights. Curr Opin Immunol 2012; 24:431-437. - 45.
Subbian S, Tsenova L, Yang G et al, Chronic pulmonary cavitary tuberculosis in rabbits: a failed host immune response. Open Biol 2011; 1:110016. - 46.
Leistikow RL, Morton RA, Bartek IL et al, The Mycobacterium tuberculosis DosR regulon assists in metabolic homeostasis and enables rapid recovery from non-respiring dormancy. J Bacteriol 2010; 192:1662. - 47.
Ramakrishnan L, Revisiting the role of the granuloma in tuberculosis. Nat Rev Immunol 2012; 12:352-366. - 48.
Lin PL, Flynn JL, Understanding latent tuberculosis: a moving target. J Immunol 2010; 185:15. - 49.
Tu HAT, Vu HD, Rozenbaum MH et al, A review of the literature on the economics of vaccination against TB. Expert Rev Vaccines 2012; 11(3):303-317. - 50.
Guo S, Zhao J, Immunotherapy for tuberculosis: what’s the better choice? Front Biosci 2012; 17:2684-2690. - 51.
Ota MOC, Odutola AA, Owlafe PK et al, Immunogenicity of the tuberculosis vaccine MVA85A is reduced by coadministration with EPI vaccines in a randomized controlled trial in Gambian infants. Sci Transl Med 2011; 3:88ra56. - 52.
Ly LH, McMurray DN, Tuberculosis: vaccines in the pipeline. Expert Rev Vaccines 2008, 7(5):635-650. - 53.
Ernst JD et al, Meeting report: The international conference on human immunity to tuberculosis. Tuberculosis 2012; DOI: 10.1016/j.tube.2012.05.003. - 54.
El Baghdadi J, Orlova M, Alter A et al, An autosomal dominant major gene confers predisposition to pulmonary tuberculosis in adults. J Exp Med 2006; 203:1679-1684. - 55.
Wang D, Zhou Y, Ji L et al, Gene polymorphisms with tuberculosis susceptibility in Li population in China. PLoS One 2012; 7(3):e33051.