What is Humoral Immunity

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In primary infection with Salmonella, it has been reported—without consideration of Salmonella‘s functions—that humoral immunity plays no role in the clearance of bacteria. In fact, Salmonella targets and suppresses several aspects of humoral immunity, including B cell lymphopoiesis, B cell activation, and IgG production. In particular, the suppression of IgG-secreting plasma cell maintenance allows the persistence of Salmonella in tissues. Therefore, the critical role(s) of humoral immunity in the response to Salmonella infection, especially at the late phase, should be re-investigated. The suppression of IgG plasma cell memory strongly hinders vaccine development against non-typhoidal Salmonella (NTS) because Salmonella can also reduce humoral immune memory against other bacteria and viruses, obtained from previous vaccination or infection. We propose a new vaccine against Salmonella that would not impair humoral immunity, and which could also be used as a treatment for antibody-dependent autoimmune diseases to deplete pathogenic long-lived plasma cells, by utilizing the Salmonella‘s own suppression mechanism of humoral immunity.

Introduction

The immune system, i.e., innate and adaptive immunity, can overcome many types of bacterial infections. The frontline against infection with bacteria such as Salmonella is innate immunity. Salmonella infection leads to enteric fever or diarrhea, often resulting in the death of humans and animals. The pathogenesis of infection should be separately considered as two dynamics of the immune system vs. Salmonella: firstly, bacterial growth within 1 week after infection and, secondly, if protected from death, bacterial clearance after 1 week after infection. Early bacterial growth in mice is controlled by the Nramp gene, expressed in macrophages, and is suppressed by a T-cell-independent host response which requires granuloma formation and production of nitric oxide and cytokines such as tumor necrosis factor α (TNFα), interleukin 12 (IL-12) and interferon γ (IFNγ) (2–6). For clearance of the bacteria, innate immunity, namely the complement system and phagocytosis by macrophages, neutrophils, and dendritic cells, are the most critical responses against bacterial pathogens, while IFNγ and antibodies resulting from adaptive immunity also dramatically enhance the innate immune response. It has been thought that adaptive immunity itself dominantly works for secondary infection except for IFNγ from T cells. However, it remains enigmatic how adaptive immunity contributes to the clearance of Salmonella in the primary infection. We herein discuss the roles of humoral immunity against Salmonella for the clearance of the bacteria.

Developing a Vaccine Against Salmonella

Salmonella enterica is a Gram-negative intracellular bacterium with over 2,500 different serovars identified until now. Salmonella Typhi (S. Typhi) and S. Paratyphi cause typhoid fever, a systemic febrile illness only affecting humans. The other numerous NTS serovars such as S. Typhimurium and S. Enteritidis infect many different hosts and results in diarrheal disease. NTS also causes severe, extra-intestinal, invasive bacteremia, referred to as invasive NTS (iNTS) disease. Immunocompromised individuals, including those infected with human immunodeficiency virus (HIV) or malaria, and infants are particularly at risk of acquiring iNTS disease (8–12). iNTS disease is estimated to cause 3.4 million cases of illness and 681,316 deaths annually, with 63.7% of all cases occurring in children under the age of five. Thus, infection with NTS is still a serious health concern. Moreover, the emergence of multidrug-resistant strains of Salmonella calls into question the future use of antibiotics to treat infection and further emphasizes the need for the development of safer and more effective vaccines. While a vaccine against NTS is not currently available, it has been reported that naturally acquired antibodies against NTS reduce the risk of iNTS disease. In contrast, infection with S. Typhi can be prevented by vaccination with attenuated strains, e.g., Ty21a. However, effective vaccines preventing iNTS disease are likely to differ from those protecting against S. Typhi infections. Furthermore, it is known that Salmonella generates chronic carriers; a chronic carrier state has been identified in 2.2% of patients with reported NTS, lasting from 30 days to 8.3 years. Although Salmonella invades myeloid cells and escapes phagocytosis, it is unclear why humoral immunity does not contribute to the clearance of Salmonella which continuously transfers among short-lived myeloid cells. Overall, the lack of a vaccine and the presence of chronic carriers suggests that NTS suppresses long-lasting humoral immunity, i.e., humoral memory.

The Immune System vs. Salmonella

Infection of susceptible Nramp mice with S. Typhimurium provides a murine model for typhoid fever which bears many similarities to human S. Typhi infection. This S. Typhi model is ultimately fatal due to the inability of such mice to restrict bacterial growth in vivo. Administration of attenuated strains of S. Typhimurium as a model of vaccination resulted in the generation of immune memory against Salmonella and protection against death from challenge with a virulent strain of the bacteria. The murine model infected with virulent S. Typhimurium showed similar pathogenesis on the early growth of bacteria. However, it seems unclear whether the model with attenuated S. Typhimurium really mimics the clearance of Salmonella, i.e., whether S. Typhi and S. Typhimurium are excluded from their hosts in a similar way. Many studies have discussed typhoidal disease using NTS strains based on the assumption that S. Typhi and S. Typhimurium utilize the same invasion system in the hosts. However, it is impossible to compare the mechanism on the clearance of Salmonella in vivo, because S. Typhi is not infectious in mice. If S. Typhi and S. Typhimurium are excluded by distinct bacterial clearances, the difference may affect the ability to generate vaccines against S. Typhi and S. Typhimurium.

Innate cells can have several roles to play during the early stage of an infection, including controlling bacterial replication and producing cytokines and chemokines that activate and recruit inflammatory cells to the site of infection. Macrophages, neutrophils and dendritic cells increase in number early after Salmonella infection and produce cytokines that are important for host survival, such as TNFα. All three phagocytic cell types also harbor bacteria during infection. IFNγ from natural killer cells at the very early infection phase and from T cells at the late infection phase can activate macrophages and promote phagocytosis. In addition to innate cells, the clearance of bacteria from the tissues also requires functional CD4 T cells, resulting in long-lasting specific immunity to re-challenge infection Susceptible mice can resolve a primary infection with attenuated Salmonella strains which requires a functioning immune system that can develop a T-bet-dependent Th1 cell response and IFNγ production to activate infected macrophages (. Similarly, mice lacking IL-12, IFNγ, reactive oxygen species, or inducible nitric oxide, all have deficiencies in the primary clearance of Salmonella. In contrast, mice lacking B cells resolve primary infection with attenuated bacterial strains with similar kinetics to wildtype mice, indicating that B-cell responses do not participate in the primary clearance of the bacteria. CD8 T cells are generally not thought to contribute to the primary clearance of attenuated Salmonella, based on studies using β2-microglobulin-deficient mice that lack class I-restricted CD8 T cells. However, recent experiments in mice lacking classical MHC class Ia genes, perforin, or granzyme, show that CD8 T cells make a modest contribution to Salmonella clearance during the later stages of the primary response. Overall, these data suggest a primary role for CD4 Th1 cells, a modest role for CD8 T cells and no role for B cells in primary immunity to Salmonella. However, the roles of adaptive immunity were considered from the viewpoint of how the lymphocytes respond to the infection, without any consideration of how Salmonella may purposefully subvert the immune response for its own advantage.

Humoral Immunity vs. Salmonella

Immunization and infection with Salmonella greatly affect hematopoiesis in a TNFα- and CXCL12-dependent manner. Salmonella is known to activate myelopoiesis and suppress B lymphopoiesis. Interestingly, the disruption of B lymphopoiesis has been also reported on Plasmodium infection in mice, suggesting a similar mechanism to Salmonella. This dramatic change in cellular commitment/differentiation is very reasonable because, in the early phase of infection, the immune system requires as many innate cells as possible to fight against the infection. Expanded myeloid cells are able to kill a lot of Salmonella, but some become the host cells for Salmonella without phagocytosis. Furthermore, the provision of B cells to the periphery is impaired due to the death of B cell precursors in the bone marrow (BM), resulting in an indirect advantage to Salmonella for their long-term persistence.

In general, antibodies can protect against bacteria mainly by facilitating the uptake of the pathogen by phagocytic cells, which then destroy the ingested bacteria. Antibodies do this in two ways: one is to coat the pathogen to be recognized by Fc receptors on phagocytic cells, which is called opsonization. Alternatively, antibodies binding to the surface of a pathogen can activate the proteins of the complement system. Complement activation results in the opsonization of the pathogen by binding complement receptors on phagocytes. Other complement components recruit phagocytic cells to the site of infection, and the terminal components of complement can lyse certain microorganisms directly by forming pores in their membranes. Most intracellular pathogens spread by moving from cell to cell through the extracellular fluids. The extracellular spaces are protected by humoral immunity. Antibodies produced by plasma cells cause the destruction of extracellular microorganisms and therefore prevent the spread of intracellular infections. Phagocytes, Salmonella‘s hosts, are short-lived and survive for 0.75 days (neutrophils, lifespan), 18–20 h (phagocytic monocytes, half-life), 1.5–2.9 days (dendritic cells, half-life), and <7 days (peripheral macrophages, lifespan). Therefore, in order to survive, Salmonella has to transfer into new host cells every 1–7 days passing through extracellular fluids containing antibodies. It is unknown how and why Salmonella can escape from antibodies in extracellular spaces when transferring into new host cells. In secondary immune responses, anti-Salmonella IgG is critical for the enhancement of phagocytosis. However, anti-Salmonella IgG in the late phase of the primary immune response does not contribute to the clearance of the bacteria. This raises the following questions: what is the difference of anti-Salmonella antibodies in the primary and secondary immune responses? Is the affinity and/or amount of antibodies important? What other functions of Salmonella have to be also considered in the subversion of the immune response?

The activation of B cells and their differentiation into long-lived plasma cells is triggered by antigen and usually requires CD4 T cell help, presenting antigen on MHC class II. Bayer-Santos and his colleagues showed that a Salmonella protein, SteD depletes surface MHC class II and inhibits T cell activation. SteD localized in the Golgi network and vesicles containing the E3 ubiquitin ligase MARCH 8 and MHC class II causing MARCH8-dependent ubiquitination and depletion of surface MHC class II and B7-2. A subset of effector CD4 T cells, known as T follicular helper cells, also control isotype switching and have a role in initiating somatic hypermutation of antibody variable V-region genes for affinity maturation mainly in germinal centers (GCs) of the spleen. Cunningham et al. indicated that GC formation is delayed when infected with Salmonella. However, GC-lacking CD40L (CD154)-deficient mice can normally induce the clearance of Salmonella in tissues. The formation of GCs and the affinity of antibodies do not affect the clearance of the bacteria. Di Niro et al. showed that Salmonella induces random activation, generating only a small fraction (0.5–2%) of Salmonella-specific plasma cells, and somatic hypermutation occurred efficiently at extrafollicular sites. Although it should be investigated how the abnormal induction consequently affects the immune responses, it is very intriguing why Salmonella does not allow immune cells to utilize the standard immune activation/maturation pathways. Following GC formation, B cells can differentiate into either short-lived plasma cells, memory B cells, or long-lived plasma cells. Memory B cells persist and are important for secondary immune responses against the same pathogen. Short-lived plasma cells temporally provide IgG but do not survive for long periods of time. In contrast, long-lived plasma cells, or their precursors, migrate into the BM and persist in CXCL12-expressing stromal cells. In general, IgG is the most critical antibody isotype for the clearance of bacteria and greatly contributes to the clearance of bacteria at least in the late phase of infection. In contrast, in the clearance of Salmonella, no role of B cells which has a potential to differentiate into IgG-secreting plasma cells has been reported. The distinction led to a possibility of Salmonella-specific suppression of humoral immunity, in particular, IgG production as described below.

Salmonella Attacks the Main Source of Igg

McSorley and Jenkins showed (i) that Salmonella can similarly survive in the tissues of naive wild-type and B cell-deficient mice until day 35 after infection, suggesting that antibodies and B cells are not necessary for the clearance of Salmonella, and (ii) that injection of heat-killed Salmonella induces a provision of anti-Salmonella IgG from day 20, although data of anti-Salmonella IgG titers in mice infected with live Salmonella are lacking. However, if Salmonella actively suppresses B cell functions, the necessity of B cells for fighting the infection, therefore, fails to be evaluated by these studies. Very recently, we have shown that Salmonella inhibits the persistence of IgG-secreting plasma cells in the BM of mice, which are the main source of serum IgG, by secreting a Salmonella protein known as SiiE. Mice infected with a SiiE-deficient strain markedly enhanced the provision of anti-Salmonella IgG and promoted the clearance of Salmonella, even in the primary infection. Given these results, the roles of antibodies and B/plasma cells, therefore, have to be re-evaluated.

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